B.Braun Melsungen AG

FDA Regulatory Profile

B.Braun Melsungen AG appears in FDA public data with 0 recalls, 5 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on April 28, 2017.

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K163358Introcan Safety 3 Closed IV CatheterApril 28, 2017
K152050PencylcapMarch 2, 2016
K131040EXTAVIPRO STERICAN 30GJuly 15, 2013
K111236INTROCAN SAFETY (R) 3 CLOSED IV CATHETER 18GA X 1-3/4 (45MM) AND 18GA X 1-1/4 (32MM) / 20GA X 1-1/4 August 30, 2011
K102033COMBITRANS MONITORING SETS AND ACCESSORIESApril 7, 2011