Diagnostics makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of Becton DickinsonLabelled 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 Becton Dickinson Diagnostic Instrument Systems with 13 510(k) clearances. The most recent is a 510(k) clearance dated Nov 21, 1996: BACTEC FUNGAL MEDIUM.
| Nov 21, 1996 | BACTEC FUNGAL MEDIUMK954923 · JTA | 510(k) clearances |
| Aug 21, 1996 | BBL MGIT PRODUCTSK954932 · MDB | 510(k) clearances |
| Aug 8, 1996 | BACTEC 9050 SYSTEMK962210 · MDB | 510(k) clearances |
| May 21, 1996 | BACTEC(R) 9000TB SYSTEMK946268 · MDB | 510(k) clearances |
| May 17, 1996 | QBC ACCUTUBE(423406)/QBC AUTOREAD(424571)K960827 · GKZ | 510(k) clearances |
| Feb 16, 1996 | BACTEC PEDS PLUS/F CULTURE VIALSK954927 · MDB | 510(k) clearances |
| Feb 16, 1996 | BACTEC CULTURE VIALS, LYTIC, ANAEROBICK954930 · MDB | 510(k) clearances |
| Feb 16, 1996 | BACTEC LYTIC/10 ANAEROBIC/F CULTURE VIALSK954925 · MDB | 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
