DistributorLabelled 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 Scientific Products with 28 510(k) clearances. The most recent is a 510(k) clearance dated Dec 24, 1986: INFECTIOUS TISSUE KIT.
| Dec 24, 1986 | INFECTIOUS TISSUE KITK864824 · | 510(k) clearances |
| Oct 23, 1984 | BLOOD DILUTION VIALK844042 · GKL | 510(k) clearances |
| Jul 19, 1983 | GLUCOSE REAGENT B6360-11K831634 · CGA | 510(k) clearances |
| Jul 7, 1983 | UREA NITROGEN-BUN-REAGENTS B6370-11AK831626 · CDQ | 510(k) clearances |
| Jul 7, 1983 | UREA NITROGEN-BUN-REAGENTS B6360-12K831625 · CDQ | 510(k) clearances |
| Jul 6, 1983 | CREATININE REAGENTS B6360-10K831627 · CGX | 510(k) clearances |
| Jul 6, 1983 | GLUCOSE REAGENT KITS-B6370-10AK831624 · CGA | 510(k) clearances |
| Jul 6, 1983 | CREATININE REAGENTS B6370-13K831628 · CGX | 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
