FirmLabelled 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 American Bioproducts with 79 510(k) clearances. The most recent is a 510(k) clearance dated Nov 12, 1998: STAR AUTOMATED MULTI-PARAMETRIC ANALYZER.
| Nov 12, 1998 | STAR AUTOMATED MULTI-PARAMETRIC ANALYZERK983460 · JPA | 510(k) clearances |
| Aug 19, 1997 | ASSERACHROM TPA TEST KITK971519 · GGP | 510(k) clearances |
| Jun 26, 1997 | STA-LIATEST D-DI TEST KITK964728 · DAP | 510(k) clearances |
| Jun 26, 1997 | STA LIATEST CONTROL [N]+[P] KITK964716 · GGN | 510(k) clearances |
| May 23, 1997 | STA D-DI CALIBRATOR KITK964718 · DAP | 510(k) clearances |
| Oct 25, 1996 | STA - LIATEST VWF TEST KITK962675 · GJT | 510(k) clearances |
| Sep 13, 1996 | STA-VWF CALIBRATOR KITK962671 · GJT | 510(k) clearances |
| Jul 23, 1996 | STA - VWF CONTROL [N]+[P] KITK962674 · GGN | 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
