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Urometrics, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
DEN000006EROS-CLITORAL THERAPY DEVICE (CTD)April 28, 2000
K980627NEVA SYSTEMApril 7, 1998
K971790KNOLL/MIDUS (MALE IMPOTENCE DIAGNOSTIC ULTRASONIC SYSTEM)December 17, 1997