Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Microprobe Corp. with 6 510(k) clearances. The most recent is a 510(k) clearance dated Jun 18, 1993: AFFIRM(TM) VPIII MICROBIAL IDENT TEST FOR CANDIDA.
| Jun 18, 1993 | AFFIRM(TM) VPIII MICROBIAL IDENT TEST FOR CANDIDAK931151 · MLA | 510(k) clearances |
| Jun 15, 1993 | AFFIRM VPIII MICROBIAL IDENTIFICATION TESTK931374 · MLA | 510(k) clearances |
| Sep 25, 1992 | AFFIRM/VP IDENT.TEST G.VAGINALIS & T.VAGINALISK923133 · MJM | 510(k) clearances |
| Sep 25, 1992 | AFFIRM VP MICROBIAL ID TEST FOR TRICHOMONAS VAGINAK922457 · MJK | 510(k) clearances |
| Jul 30, 1992 | AFFIRM VP SAMPLE COLLECTION SETK920536 · LIO | 510(k) clearances |
| Jul 30, 1992 | AFFIRM PROCESSORK923268 · JQW | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
