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Biorem
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K833454
BIOREM 3000 & 4000
February 21, 1984
K822099
BIOREM 2000
August 27, 1982