Bd Becton Dickinson Vacutainer Systems Preanalytic - FDA 510(k) Clear...
632
Total
625
Cleared
0
Denied
Bd Becton Dickinson Vacutainer Systems Preanalytic has 625 FDA 510(k) cleared medical devices. Based in Washington, US.
Historical record: 625 cleared submissions from 1976 to 2001.
Browse the FDA 510(k) cleared devices submitted by Bd Becton Dickinson Vacutainer Systems Preanalytic Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Bd Becton Dickinson Vacutainer...
632 devices
Cleared
Jun 06, 2001
BACTEC MGIT 960 SIR KITS
Microbiology
247d
Cleared
Mar 21, 2001
0.9% SODIUM CHLORIDE INJECTION, USP BD PRE-FILLED FLUSH SYRINGE
General Hospital
124d
Cleared
Feb 01, 2001
BD VACUTAINER PASSIVE SHIELDING BLOOD COLLECTION NEEDLE
General Hospital
86d
Cleared
Nov 29, 2000
B-D ULTRA-FINE III PEN NEEDLE
General Hospital
69d
Cleared
Jun 28, 2000
BD DIRECTIGEN FLU A+B
Microbiology
58d
Cleared
Apr 25, 2000
MOXIFLOXACIN, 5 UG, BBL SENSI-DISC
Microbiology
48d
Cleared
Apr 13, 2000
GATIFLOXACIN, 5 UG, BBL SENSI-DISC
Microbiology
30d
Cleared
Nov 03, 1999
SYNERCID, 15 UG, BBL SENSI-DISC
Microbiology
42d
Cleared
Oct 01, 1999
BECTON DICKINSON SYRINGE
General Hospital
49d
Cleared
Sep 23, 1999
VACUTAINER BRAND SODIUM CITRATE PEDIATRIC TUBE
Chemistry
143d
Cleared
Sep 23, 1999
QBC STAR CENTRIFUGAL HEMATOLOGY SYSTEM
Hematology
30d
Cleared
Apr 09, 1999
ANGIOCATH AUTOGUARD CATHETER, INSYTE AUTOGUARD CATHETER
General Hospital
147d
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