Company ยท US
Becton Dickinson Diagnostic Instrument Systems
FDA 510(k) clearances and medical device recalls filed under this name, 1995 to 1996. Name variants (Inc, Corp, punctuation) are merged.
13510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Nov 21, 1996 | K954923 | BACTEC FUNGAL MEDIUM Becton Dickinson Diagnostic Instrument Systems | JTA |
| Aug 21, 1996 | K954932 | BBL MGIT PRODUCTS Becton Dickinson Diagnostic Instrument Systems | MDB |
| Aug 8, 1996 | K962210 | BACTEC 9050 SYSTEM Becton Dickinson Diagnostic Instrument Systems | MDB |
| May 21, 1996 | K946268 | BACTEC(R) 9000TB SYSTEM Becton Dickinson Diagnostic Instrument Systems | MDB |
| May 17, 1996 | K960827 | QBC ACCUTUBE(423406)/QBC AUTOREAD(424571) Becton Dickinson Diagnostic Instrument Systems | GKZ |
| Feb 16, 1996 | K954930 | BACTEC CULTURE VIALS, LYTIC, ANAEROBIC Becton Dickinson Diagnostic Instrument Systems | MDB |
| Feb 16, 1996 | K954927 | BACTEC PEDS PLUS/F CULTURE VIALS Becton Dickinson Diagnostic Instrument Systems | MDB |
| Feb 16, 1996 | K954925 | BACTEC LYTIC/10 ANAEROBIC/F CULTURE VIALS Becton Dickinson Diagnostic Instrument Systems | MDB |
| Feb 16, 1996 | K954921 | BACTEC STANDARD/10 AEROBIC/F CULTURE VIALS Becton Dickinson Diagnostic Instrument Systems | MDB |
| Feb 8, 1996 | K954924 | BACTEC PEDS PLUS CLUTURE VIALS Becton Dickinson Diagnostic Instrument Systems | MDB |
| Feb 5, 1996 | K955504 | QBC ACCUREAD SYSTEM Becton Dickinson Diagnostic Instrument Systems | GKZ |
| Oct 5, 1995 | K953340 | QBC ACCUTUBE Becton Dickinson Diagnostic Instrument Systems | GKZ |
| Sep 25, 1995 | K945205 | QBC ACCUTUBE Becton Dickinson Diagnostic Instrument Systems | GKZ |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||