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Buckman Consultants
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K830316
UNIFLEX
March 24, 1983
K823882
M-BRACE
January 17, 1983
K821829
UROGARD
July 30, 1982