B.Braun Melsungen AG is one of 13015 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
B.Braun Melsungen AG - FDA 510(k) Cleared Devices
Recent clearances: Introcan Safety 3 Closed IV Catheter, Pencylcap, EXTAVIPRO STERICAN 30G
5
Total
5
Cleared
0
Denied
B.Braun Melsungen AG has 5 FDA 510(k) cleared medical devices. Based in Allentown, US.
Historical record: 5 cleared submissions from 2011 to 2017. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by B.Braun Melsungen AG Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by B.Braun Medical, Inc. and Yes Medical Device Services GmbH.
FDA 510(k) Regulatory Record - B.Braun Melsungen AG
5 devices
Cleared
Apr 28, 2017
Introcan Safety 3 Closed IV Catheter
General Hospital
149d
Cleared
Mar 02, 2016
Pencylcap
General Hospital
223d
Cleared
Jul 15, 2013
EXTAVIPRO STERICAN 30G
General Hospital
91d
Cleared
Aug 30, 2011
INTROCAN SAFETY (R) 3 CLOSED IV CATHETER 18GA X 1-3/4 (45MM) AND 18GA X 1-1/4...
General Hospital
120d
Cleared
Apr 07, 2011
COMBITRANS MONITORING SETS AND ACCESSORIES
Cardiovascular
262d