Becton, Dickinson and Co. is one of 13017 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Becton, Dickinson and Co. - FDA 510(k) Cleared Devices
Recent clearances: BD Veritor System for the Rapid Detection of Flu A + B CLIA waived kit, BD Veritor System for the Rapid Detection of Flu A + B Laboratory kit, BD PHOENIX AUTOMATED MICROBIOLOGY SYSTEM-PIPERCILLIN (GN) 0.5-128 UG/ML
6
Total
6
Cleared
0
Denied
Becton, Dickinson and Co. has 6 FDA 510(k) cleared medical devices. Based in Sarasota, US.
Historical record: 6 cleared submissions from 2001 to 2015. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Becton, Dickinson and Co. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Becton, Dickinson and Co.
6 devices
Cleared
Oct 27, 2015
BD Veritor System for the Rapid Detection of Flu A + B CLIA waived kit
Microbiology
27d
Cleared
Oct 27, 2015
BD Veritor System for the Rapid Detection of Flu A + B Laboratory kit
Microbiology
27d
Cleared
Apr 15, 2010
BD PEN NEEDLE
General Hospital
101d
Cleared
Aug 12, 2004
BD PHOENIX AUTOMATED MICROBIOLOGY SYSTEM-PIPERCILLIN (GN) 0.5-128 UG/ML
Microbiology
59d
Cleared
Apr 19, 2001
BD ULTRA-FINE II INSULIN SYRINGE-MINI NEEDLE, MODEL 30G * 3/16 (5MM)
General Hospital
24d
Cleared
Mar 12, 2001
BD VISIDRAPE OPHTHALMIC DRAPES
General Hospital
14d