Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Amico Laboratories, Inc. with 33 510(k) clearances. The most recent is a 510(k) clearance dated Oct 7, 1991: AMIZYME EPSTEIN-BARR VIRUS (EBV) IGM ANTIBODY TEST.
| Oct 7, 1991 | AMIZYME EPSTEIN-BARR VIRUS (EBV) IGM ANTIBODY TESTK911362 · LJN | 510(k) clearances |
| Dec 12, 1985 | ANTI-EPSTEIN-BARR VIRUS KITK842662 · GNP | 510(k) clearances |
| Dec 6, 1985 | ANTI-HERPES SIMPLEX VIRUS TYPE 1 OR 2K842663 · GQO | 510(k) clearances |
| Dec 6, 1985 | AMIZYME-CMV KITK842529 · GQI | 510(k) clearances |
| Dec 6, 1985 | ANTI-CYTOMEGALOVIRUS KITK842661 · GQI | 510(k) clearances |
| Dec 6, 1985 | AMIZYME-HSV TYPES 1 & 2 TEST KITSK842531 · GQO | 510(k) clearances |
| Dec 6, 1985 | AMIZYME-EBV TEST KITK842530 · GNP | 510(k) clearances |
| Oct 30, 1984 | ANTI-SCHISTOSOMA SPECIES KITK842660 · GNH | 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
