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 14, 2026, FDA's public records list Bio/Data Corp. with 37 510(k) clearances. The most recent is a 510(k) clearance dated Jul 12, 2000: MICROSAMPLE COAGULATION ANALYZER, MODEL MCA 310-C.
| Jul 12, 2000 | MICROSAMPLE COAGULATION ANALYZER, MODEL MCA 310-CK001891 · GKP | 510(k) clearances |
| Mar 24, 1995 | MICROSAMPLE COAGULATION ANALYZERK943153 · GKP | 510(k) clearances |
| Jun 23, 1989 | PLATELET AGGREGATION PROFILER MODEL PAP-4CK893650 · JPA | 510(k) clearances |
| Mar 28, 1988 | KINETIC FIBRINOGEN ASSAYK881150 · GIS | 510(k) clearances |
| Nov 20, 1987 | PLATELET EXTRACT REAGENTK873382 · GGW | 510(k) clearances |
| Mar 18, 1986 | VON WILLEBRAND FAC. DEFIC. ABNORMAL CONTROL PLASMAK860751 · JPK | 510(k) clearances |
| Mar 4, 1986 | MICROSAMPLE COAGULATION ANALYSER, MODEL 110WPK860342 · JPA | 510(k) clearances |
| Jan 7, 1986 | MICROSAMPLE COAGULATION ANALYSER MODEL 110PK854546 · JPA | 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
