Form 8-K - Current report
January 02 2024 - 8:52AM
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UNITED
STATES
SECURITIES
AND EXCHANGE COMMISSION
Washington,
D.C. 20549
FORM
8-K
CURRENT
REPORT
Pursuant
to Section 13 OR 15(d) of The Securities Exchange Act of 1934
Date
of Report (Date of earliest event reported) January 2, 2024
Daxor
Corporation
(Exact
name of registrant as specified in its charter)
New
York |
|
811-22684 |
|
13-2682108 |
(State
or other jurisdiction |
|
(Commission |
|
(IRS
Employer |
of
incorporation) |
|
File
Number) |
|
Identification
No.) |
109
Meco Lane, Oak Ridge, TN |
|
37830 |
(Address
of principal executive offices) |
|
(Zip
Code) |
212-330-8500
Registrant’s
telephone number, including area code
(Former
name or former address, if changed since last report.)
Check
the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under
any of the following provisions ( see General Instruction A.2. below):
☐ |
Written
communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425) |
|
|
☐ |
Soliciting
material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12) |
|
|
☐ |
Pre-commencement
communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b)) |
|
|
☐ |
Pre-commencement
communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c)) |
Securities
registered pursuant to Section 12(b) of the Act:
Title
of each class |
|
Trading
Symbol(s) |
|
Name
of each exchange on which registered |
Common
Stock $0.01 par value |
|
DXR |
|
Nasdaq |
Indicate
by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§230.405
of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§240.12b-2 of this chapter).
Emerging
growth company ☐
If
an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying
with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. ☐
Potential
persons who are to respond to the collection of information contained in this form are not required to respond unless the form displays
a currently valid OMB control number.
Item
8.01 – Other Events
On
January 2, 2024 Daxor Corporation announced it has submitted its next-generation blood volume analyzer - Daxor BVA - to the U.S. Food
and Drug Administration (FDA) via the 510(k)/CLIA-waiver dual submission pathway. Potential clearance is expected during the first half
of 2024. The Company’s mission is to advance healthcare by enabling optimal fluid management. The press release issued is attached
to this filing as Exhibit 99.1
Item
9.01 Exhibits
(d)
Exhibits. The following exhibit is filed with this Current Report on Form 8-K:
SIGNATURES
Pursuant
to the requirements of the Securities Exchange Act of 1934, the Registrant has duly caused this report to be signed on its behalf by
the undersigned, hereunto duly authorized.
|
DAXOR CORPORATION |
|
(Registrant) |
|
|
|
Date:
January 2, 2024 |
By: |
/s/
Robert J. Michel |
|
Name: |
Robert
J. Michel |
|
Title: |
Chief
Financial Officer |
Exhibit
99.1
Daxor
Corporation Submits Dual 510(k)/CLIA-waiver Application to the FDA for Its Advanced Next-Generation Blood Volume Analyzer
The
New BVA System is Designed to be Significantly Faster, Simpler and Give Results at the Bedside
Oak
Ridge, TN – January 2, 2024 -- Daxor Corporation (Nasdaq: DXR), the global leader in blood volume measurement technology,
today announces it has submitted its next-generation blood volume analyzer - Daxor BVA - to the U.S. Food and Drug Administration (FDA)
via the 510(k)/CLIA-waiver dual submission pathway. Potential clearance is expected during the first half of 2024. The Company’s
mission is to advance healthcare by enabling optimal fluid management.
The
new Daxor BVA device directly quantifies the intravascular blood, red blood cell and plasma volume, providing clinicians with actionable
information to achieve optimal fluid management for their patients. Compared to the current Daxor BVA-100 system, the new Daxor BVA is
designed to be three times faster, simpler to operate, completely portable, and capable of performing bedside analysis, making it easier
for healthcare providers to integrate this innovative diagnostic into their clinical workflow.
“Today
marks a long-anticipated and momentous milestone in our continued commitment to our customers, patients, and to achieving our vision
of optimal blood volume for all,” said Michael Feldschuh, Daxor’s CEO and President. “Funded under contract by the
U.S. Department of Defense, our next-generation analyzer will deliver a level of speed, access, and accuracy to blood volume management
that can significantly improve care and outcomes in medicine.”
About
Daxor Corporation
Daxor
Corporation (Nasdaq: DXR), is the global leader in blood volume measurement technology focused on blood volume testing innovation.
We developed and market the BVA-100® (Blood Volume Analyzer), the only diagnostic blood test cleared by the FDA to
provide safe, accurate, objective quantification of blood volume status and composition compared to patient-specific norms. Over
65,000+ tests have been performed at leading hospital centers across the U.S., enhancing hospital performance metrics in a broad
range of surgical and medical conditions, including significantly reducing mortality and readmissions in heart failure and critical
care. Daxor has several ongoing trials in the areas of heart failure treatment with support from the NIH and is under contract
developing analyzers to improve combat casualty care with the U.S. Department of Defense. Daxor’s mission is to advance
healthcare by enabling optimal fluid management with blood volume analysis. Daxor’s vision is optimal blood volume for all.
For more information, please visit our website at Daxor.com. Sign up to receive news on Daxor’s innovative technology HERE.
Forward-Looking
Statements
Certain
statements in this release may include forward-looking statements within the meaning of the Private Securities Litigation Reform Act
of 1995, including without limitation, statements regarding the impact of hiring sales staff and expansion of our distribution channels.
Forward-looking statements are predictions, projections and other statements about future events that are based on current expectations
and assumptions and, as a result, are subject to risks and uncertainties. Many factors could cause actual future events to differ materially
from the forward-looking statements in this release, including, without limitation, those risk associated with our post-market clinical
data collection activities, benefits of our products to patients, our expectations with respect to product development and commercialization
efforts, our ability to increase market and physician acceptance of our products, potentially competitive product offerings, intellectual
property protection, FDA regulatory actions, our ability to integrate acquired businesses, our expectations regarding anticipated synergies
with and benefits from acquired businesses, and additional other risks and uncertainties described in our filings with the SEC. Forward-looking
statements speak only as of the date when made. Daxor does not assume any obligation to publicly update or revise any forward-looking
statements, whether as a result of new information, future events or otherwise.
Investor
Relations Contact:
Bret
Shapiro
Sr.
Managing Partner, CORE IR
1-516-222-2560
brets@coreir.com
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