ITEM 7.01. REGULATION FD DISCLOSURE.

On December 4, 2012, the Company issued a press release entitled "Chembio to Present at LD Micro V: Main Event Conference". A copy of the press release is furnished herewith as Exhibit 99.1.

On November 28, 2012, the Company was informed by the US Food and Drug Administration ("FDA") that its premarket approval ("PMA") application for the DPP(R) HIV 1/2 Assay lacked certain information needed to complete its FDA's review. The two issues that were cited involved manufacturing-related issues (validation on one piece of equipment and additional samples for in-process testing) and did not involve any clinical trial data. The Company has addressed the issue concerning samples for the in-process testing, and expects to complete the equipment validation today and submit them to the FDA by the end of this week. If the Company does not submit data satisfactory to the FDA by December 7, 2012, then the approval process can be delayed up to an additional 180 days. The Company believes this delay will not occur, and it will receive approval before the end of the year.

The information in this Item 7.01 of this Form 8-K is being furnished and shall not be deemed "filed" for the purposes of Section 18 of the Securities Exchange Act of 1934, or otherwise subject to the liabilities of that section. The information in this Item 7.01 of this Form 8-K also shall not be deemed to be incorporated by reference into any filing under the Securities Act of 1933, as amended, or the Securities Exchange Act of 1934, except to the extent that the Company specifically incorporates it by reference.

ITEM 9.01. FINANCIAL STATEMENTS AND EXHIBITS

Exhibits.

99.1 Press Release entitled "Chembio to Present at LD Micro V:
Main Event Conference" dated December 4, 2012.

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