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 15, 2026, FDA's public records list Analytical Products with 57 510(k) clearances. The most recent is a 510(k) clearance dated Mar 11, 1993: API 20E/UNISCEPT 20E.
| Mar 11, 1993 | API 20E/UNISCEPT 20EK924814 · JSS | 510(k) clearances |
| Dec 3, 1992 | API UNISCEPT MIC/TYPE 2 AND 3 AND MICRO MICK923684 · JWY | 510(k) clearances |
| Oct 13, 1992 | API UNISCEPT KB/TYPE 2 AND 3K922926 · JWY | 510(k) clearances |
| Sep 10, 1990 | MODIFICATION TO API UNISCEPT 20GPK901559 · LQL | 510(k) clearances |
| Apr 16, 1990 | DMAC INDOLE REAGENTK901390 · JTO | 510(k) clearances |
| Nov 13, 1989 | API UNISCEPT KBK895796 · JWY | 510(k) clearances |
| Nov 22, 1988 | MODIFICATION MIC/API UNISCEPT(R)K884509 · JWY | 510(k) clearances |
| Nov 22, 1988 | MODIFICATION MICRO-MICK884510 · JWY | 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
