Diagnostics 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 Alamar with 7 510(k) clearances. The most recent is a 510(k) clearance dated May 8, 1991: ANTIMICROBIAL SUSCEPT. TEST PANEL (CEFTIZOXIME).
| May 8, 1991 | ANTIMICROBIAL SUSCEPT. TEST PANEL (CEFTIZOXIME)K911391 · JWY | 510(k) clearances |
| May 8, 1991 | ANTIMICROBIAL SUSCEPT. TEST PANEL(TRIMETHOPRIM)K911390 · JWY | 510(k) clearances |
| May 8, 1991 | ANTIMICROBIAL SUSCEPTIBILITY TEST PANEL (IMIPENEM)K911389 · JWY | 510(k) clearances |
| May 8, 1991 | ANTIMICROBIAL SUSCEPTIBILITY TEST PANEL (CEFOTETANK911392 · JWY | 510(k) clearances |
| Mar 11, 1991 | ANTIMICROBIAL SUSCEPTIBILITY TEST PANELK910484 · JWY | 510(k) clearances |
| Feb 25, 1991 | ANTIMICROBIAL CEFOPERAZONEK910345 · JWY | 510(k) clearances |
| Feb 25, 1991 | ANTIMICROBIAL CEFTRIAXONEK910346 · 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
