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Frigitronics, 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
K905392
HT4-SERIES HYSTEROSCOPES AND ACCESSORIES
April 30, 1991
K905495
HYSTEROMAT HYSTEROFLATOR HYSTEROSCOPIC INSUFFLATOR
April 29, 1991
K905393
HC-SERIES MEDICAL CAMERA/LIGHT SOURCE AND ACCESSOR
January 16, 1991