Becton Dickinson Diagnostic Instrument Systems
Becton Dickinson Diagnostic Instrument Systems holds FDA 510(k) medical device clearances, first cleared 1995, most recent 1996.
Top product codes for Becton Dickinson Diagnostic Instrument Systems
Recent clearances by Becton Dickinson Diagnostic Instrument Systems
- K954923 — BACTEC FUNGAL MEDIUM
- K954932 — BBL MGIT PRODUCTS
- K962210 — BACTEC 9050 SYSTEM
- K946268 — BACTEC(R) 9000TB SYSTEM
- K960827 — QBC ACCUTUBE(423406)/QBC AUTOREAD(424571)
- K954921 — BACTEC STANDARD/10 AEROBIC/F CULTURE VIALS
- K954925 — BACTEC LYTIC/10 ANAEROBIC/F CULTURE VIALS
- K954927 — BACTEC PEDS PLUS/F CULTURE VIALS
- K954930 — BACTEC CULTURE VIALS, LYTIC, ANAEROBIC
- K954924 — BACTEC PEDS PLUS CLUTURE VIALS
- K955504 — QBC ACCUREAD SYSTEM
- K953340 — QBC ACCUTUBE
- K945205 — QBC ACCUTUBE
Data sourced from openFDA. This site is unofficial and independent of the FDA.