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20:23 EDT Biomerica begins shipping samples of 10 minute test for COVID 19 exposure Biomerica announced it has commenced shipping initial samples of its COVID 19 IgG/IgM Rapid Test to countries outside the US.sec.govTest kits are required to be FDA cleared or approved by the 510(k) or PMA processes in order to be sold with labeling For In Vitro Diagnostics Use in the U.S. BBIs first commercialized test kit, the Boston Biomedica Inc. Borrelia burgdorferi IgM and IgG Western Blot Test Kit, received 510(k) clearance in November, 2003.Form 10 K SECWe make available, free of charge, through our web site, these reports, including our annual report on Form 10 K, quarterly reports on Form 10 Q, current reports on Form 8 K, and amendments to those reports filed or furnished pursuant to Section 13(a) or 15(d) of the Securities Exchange Act of 1934, as soon as reasonably practicable after such

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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