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Bcd Products, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K831773
MAI HYDROSEAL IMPLANT FOR SCLERAL BUCK
August 16, 1983
K813547
THERMASCAN
March 12, 1982