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Medpro, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K772062
NEONATAL FLOTATION SYSTEM
November 15, 1977
K771824
MEDPRO FLOTATION SYSTEM
October 19, 1977
K760870
HEEL/ELBOW FLOTATION CUSHION
November 1, 1976
K760613
FLOTATION UNIT, CHAIR
October 14, 1976