Medical device 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 Laboratory Products with 8 510(k) clearances. The most recent is a 510(k) clearance dated Sep 12, 1983: CIN AGAR.
| Sep 12, 1983 | CIN AGARK832588 · JSJ | 510(k) clearances |
| Jan 9, 1981 | FLAME PHOTOMETRY REAGENTSK803051 · JIX | 510(k) clearances |
| Jan 2, 1981 | CHLORIDE/TCO2 ANALYZER REAGENTSK803013 · CHJ | 510(k) clearances |
| Dec 30, 1980 | SPRAY, SYNTHETIC SMEARK803050 · IFI | 510(k) clearances |
| Mar 19, 1980 | VARIOUS REAGENTS FOR BLOOD CELL ANALYZERK800180 · GIF | 510(k) clearances |
| Jan 11, 1980 | CHEMISTRY ANALYZER REAGENTSK792482 · CIX | 510(k) clearances |
| Dec 31, 1979 | CULTURE PLATES & TUBED MEDIAK792481 · JTZ | 510(k) clearances |
| Dec 18, 1979 | STAINS, COUNTERSTAINS & GEN. PURPOSEK792483 · ICL | 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
