ARCH THERAPEUTICS, INC. (OTCMKTS:ARTH) Files An 8-K Regulation FD Disclosure
Item 7.01
On December 17, 2018, Arch Therapeutics, Inc. (the “Company”) issued a press release announcing that the Company’s 510(k) premarket notification for AC5™ Topical Gel has been reviewed and cleared by the U.S. Food and Drug Administration. The text of the press release is attached hereto as Exhibit 99.1 and is incorporated by reference herein.
The disclosure under Item 7.01 (Regulation FD Disclosure) is incorporated herein by reference.
| Item 9.01 | Financial Statements and Exhibits |
(d) The following exhibits are being filed herewith:
Arch Therapeutics, Inc. Exhibit
EX-99.1 2 tv509257_ex99-1.htm EXHIBIT 99.1 Exhibit 99.1 Arch Therapeutics Receives 510(k) Clearance from the US FDA for AC5TM Topical Gel AC5™ provides a new option for the treatment of topical wounds FRAMINGHAM,…
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About ARCH THERAPEUTICS, INC. (OTCMKTS:ARTH)
Arch Therapeutics, Inc. is a development-stage company. The Company operates as a biotechnology company. The Company focuses on developing products to stop bleeding (hemostasis) and control leaking (sealant) during surgery and trauma care. The Company’s technology is based on a self-assembling peptide that creates a physical, mechanical barrier, which could be applied to seal organs or wounds that are leaking blood and other fluids. The Company’s primary product candidates, collectively known as the AC5 Devices (AC5), are designed to achieve hemostasis in surgical procedures. The Company’s product candidates rely on its self-assembling peptide technology and are designed to achieve hemostasis in skin wounds, and minimally invasive and open surgical procedures. The Company focuses on developing other product candidates based on its technology platform for use in a range of indications. As of September 30, 2016, the Company had not generated any revenues.