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Promedex, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K914407
PROMOGLASS(TM) SUNGLASSES (NON-PRESCRIPTION)
December 31, 1991
K905764
SEMINOR
March 12, 1991
K900404
VARICOSCREEN(TM)
December 7, 1990