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Frontier Products
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K831001
UNICUFF-BLOOD PRESSURE CUFF
July 28, 1983
K822305
ORTHO-LEVEL
August 20, 1982
K812639
UNICUFF
October 2, 1981
K801099
UNICUF, BLOOD PRESSURE CUFF
May 30, 1980