Becton, Dickinson Company is one of 13017 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Becton, Dickinson Company - FDA 510(k) Cleared Devices
Recent clearances: BD Ultra-Fine™ Insulin Syringe, BD Ultra-Fine™ II Insulin Syringe, BD Insulin Syringes with the BD Ultra-Fine™ needle and BD Insulin Syringes with Micro-Fine™ IV Needle, BD Phoenix Automated Microbiology System - GN Ceftazidime/avibactam (0.25/4- 32/4ug/mL), BD FlowSmart Set
3
Total
3
Cleared
0
Denied
Becton, Dickinson Company has 3 FDA 510(k) cleared medical devices. Based in Franklin Lakes, US.
Historical record: 3 cleared submissions from 2015 to 2017. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Becton, Dickinson Company Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Becton Dickinson & Company as regulatory consultant.
FDA 510(k) Regulatory Record - Becton, Dickinson Company
3 devices
Cleared
Apr 12, 2017
BD Ultra-Fine™ Insulin Syringe, BD Ultra-Fine™ II Insulin Syringe, BD Insulin...
General Hospital
63d
Cleared
Mar 21, 2017
BD Phoenix Automated Microbiology System - GN Ceftazidime/avibactam (0.25/4-...
Microbiology
88d
Cleared
Apr 28, 2015
BD FlowSmart Set
General Hospital
105d