Medical Device Manufacturer · US , Mchenry , IL

B. Braun Instruments - FDA 510(k) Cleared Devices

13 submissions · 13 cleared · Since 1976

Total

Cleared

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.

B. Braun Instruments is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - B. Braun Instruments

13 devices

1-12 of 13

Cleared Nov 02, 1976

INTRAVENOUS TRANSFER SET (INTRAFIX)

K760380 · JCY

General & Plastic Surgery · 89d

Cleared Nov 02, 1976

BLOOD TRANSFUSION SET (SANGOFIX)

K760381 · JCY

General & Plastic Surgery · 89d

Cleared Nov 02, 1976

CONNECTORS

K760382 · GCD

General & Plastic Surgery · 89d

Cleared Nov 02, 1976

STOPCOCKS

K760383 · KGZ

General & Plastic Surgery · 89d

Cleared Nov 02, 1976

STOPPERS

K760384 · KGZ

General & Plastic Surgery · 89d

Cleared Nov 02, 1976

EXTENSION SETS

K760385 · KGZ

General & Plastic Surgery · 89d

Cleared Nov 02, 1976

CENTRAL VEINOUS PRESSURE SETS

K760386 · DQO

Cardiovascular · 89d

Cleared Nov 02, 1976

CATHETER, CAVA (CAVAFIX)

K760387 · DQO

Cardiovascular · 89d

Cleared Nov 02, 1976

CATHETER, VEIN (VENOFIX)

General & Plastic Surgery · 89d

Cleared Nov 02, 1976

CATHETER, VEIN (BRAUNULA T)

K760390 · JCY

General & Plastic Surgery · 89d

Cleared Nov 02, 1976

CATHETER, VEIN (BRAUNULA)

K760391 · JCY

General & Plastic Surgery · 89d

B. Braun Instruments - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - B. Braun Instruments

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