B. Braun Instruments is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
B. Braun Instruments - FDA 510(k) Cleared Devices
13
Total
13
Cleared
0
Denied
B. Braun Instruments has 13 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 13 cleared submissions from 1976 to 1976. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by B. Braun Instruments Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - B. Braun Instruments
13 devices
Cleared
Nov 02, 1976
INTRAVENOUS TRANSFER SET (INTRAFIX)
General & Plastic Surgery
89d
Cleared
Nov 02, 1976
BLOOD TRANSFUSION SET (SANGOFIX)
General & Plastic Surgery
89d
Cleared
Nov 02, 1976
CONNECTORS
General & Plastic Surgery
89d
Cleared
Nov 02, 1976
STOPCOCKS
General & Plastic Surgery
89d
Cleared
Nov 02, 1976
STOPPERS
General & Plastic Surgery
89d
Cleared
Nov 02, 1976
EXTENSION SETS
General & Plastic Surgery
89d
Cleared
Nov 02, 1976
CENTRAL VEINOUS PRESSURE SETS
Cardiovascular
89d
Cleared
Nov 02, 1976
CATHETER, CAVA (CAVAFIX)
Cardiovascular
89d
Cleared
Nov 02, 1976
CATHETER, VEIN (VENOFIX)
Cardiovascular
89d
Cleared
Nov 02, 1976
CANNULA, IV
General & Plastic Surgery
89d
Cleared
Nov 02, 1976
CATHETER, VEIN (BRAUNULA T)
General & Plastic Surgery
89d
Cleared
Nov 02, 1976
CATHETER, VEIN (BRAUNULA)
General & Plastic Surgery
89d
Cleared
Nov 02, 1976
SYRINGES
General Hospital
89d