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B. Braun Instruments

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
13
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K760382CONNECTORSNovember 2, 1976
K760388CATHETER, VEIN (VENOFIX)November 2, 1976
K760381BLOOD TRANSFUSION SET (SANGOFIX)November 2, 1976
K760390CATHETER, VEIN (BRAUNULA T)November 2, 1976
K760384STOPPERSNovember 2, 1976
K760385EXTENSION SETSNovember 2, 1976
K760380INTRAVENOUS TRANSFER SET (INTRAFIX)November 2, 1976
K760391CATHETER, VEIN (BRAUNULA)November 2, 1976
K760386CENTRAL VEINOUS PRESSURE SETSNovember 2, 1976
K760392SYRINGESNovember 2, 1976
K760389CANNULA, IVNovember 2, 1976
K760387CATHETER, CAVA (CAVAFIX)November 2, 1976
K760383STOPCOCKSNovember 2, 1976