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 15, 2026, FDA's public records list Atlantic Antibodies with 18 510(k) clearances. The most recent is a 510(k) clearance dated May 9, 1989: SPQ TM TEST SYSTEM II FOR CRP.
| May 9, 1989 | SPQ TM TEST SYSTEM II FOR CRPK892526 · DCK | 510(k) clearances |
| Mar 16, 1989 | SPQ(TM) ANTIBODY REAGENT SET II FOR APO A-I/APO BK891154 · MSJ | 510(k) clearances |
| Mar 3, 1989 | SPQ(TM) ANTIBODY REAGENT SET II FOR TRFK890563 · DDG | 510(k) clearances |
| Feb 23, 1989 | SPQ(TM) ANTIBODY REAGENT SET II FOR IGMK890561 · CFQ | 510(k) clearances |
| Feb 22, 1989 | SPQ(TM) ANTIBODY REAGENT SET II FOR IGGK890416 · DEW | 510(k) clearances |
| Feb 22, 1989 | SPQ(TM) ANTIBODY REAGENT SET II FOR HPTK890562 · DAD | 510(k) clearances |
| Feb 17, 1989 | SPQ(TM) ANTIBODY REAGENT SET II FOR C3K890417 · KTQ | 510(k) clearances |
| Feb 17, 1989 | SPQ(TM) ANTIBODY REAGENT SET II FOR AATK890415 · DEM | 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
