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B. Braun Medizintechnologie GmbH

FDA Regulatory Profile

B. Braun Medizintechnologie GmbH appears in FDA public data with 0 recalls, 3 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on January 29, 2008.

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K072760SOLCART BJanuary 29, 2008
K071518DIACAP LO PS (10, 12, 15) AND DIACAP HI PS (10, 12, 15, 18, 20) HEMODIALYZERSAugust 17, 2007
K052764DIACAP ULTRA DIALYSIS FLUID FILTERJune 9, 2006

FDA data resources