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 BHP Diagnostix with 25 510(k) clearances. The most recent is a 510(k) clearance dated Nov 2, 1990: SERACON CR REFERENCE.
| Nov 2, 1990 | SERACON CR REFERENCEK904503 · JJX | 510(k) clearances |
| Oct 29, 1986 | SERACON CT REFERENCEK863648 · JJY | 510(k) clearances |
| Aug 19, 1986 | SERACON(TM) CAL (PRODUCT NO. DO35)K862594 · JIX | 510(k) clearances |
| Mar 22, 1985 | QUANTICEL HHR + TWO HUMAN HEMATOLOGY W/PLATELETSK844927 · JPK | 510(k) clearances |
| Mar 22, 1985 | QUANTICEL HHR TWO HUMAN HEMATOLOGY REFERENCEK844928 · JPK | 510(k) clearances |
| Nov 27, 1984 | SERACON TM SR IVK844026 · JIX | 510(k) clearances |
| Nov 27, 1984 | SERACON TM SR IIIK844027 · JIX | 510(k) clearances |
| Dec 31, 1979 | SERACON-SRI (PROD. # D029K792486 · JIX | 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
