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Bauerfeind AG
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
2
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K123921
BODYTRONIC 200
April 26, 2013
K111662
VENOTRAIN CURAFLOW
October 4, 2011