AND EXCHANGE COMMISSION
TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934
of Report (Date of earliest event reported): July 2, 2020
CENTER USA, INC.
name of registrant as specified in its charter)
or other jurisdiction of
E. University Boulevard, Tucson, AZ 85705
of Principal Executive Offices)
name or former address, if changed since last report)
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):
communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)|
material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)|
communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))|
communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))|
registered pursuant to Section 12(b) of the Act:
of each class
of Each Exchange on Which Registered|
8 - Other Events.
July 2, 2020, the Company received notice from the U.S. Food & Drug Administration (“FDA”) stating that the FDA
has reviewed the Section 510(k) premarket notification of intent to market filed by the Company’s subsidiary, Psoria-Shield,
Inc. (“PSI”), for PSI’s AURORA device and has determined that the device is substantially equivalent to legally
marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments,
that do not require approval of a premarket approval application (PMA), and may therefore, market the device, subject to the general
controls provisions of the Act. The AURORA device is indicated for use in targeted PUVA photochemistry and UVB phototherapy for
the treatment of skin conditions including psoriasis, vitiligo, atopic dermatitis (eczema), and seborrheic dermatitis. In addition,
the system UVB channel is indicated for the treatment of leukoderma.
9.01 Financial Statements and Exhibits.
Financial Statements of business acquired. None.
Pro forma financial information. None.
Shell Company Transaction. Not applicable.
Exhibits. US Food & Drug Administration Letter dated July 2, 2020
to the requirements of the Securities Exchange Act of 1934, as amended, the registrant caused this report to be signed on its
behalf by the undersigned, thereunto duly authorized.
CENTER USA, INC.|
July 6, 2020
Calvin R. O’Harrow|