FDA 510(k) Applications Submitted by UROMETRICS, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K980627 | 02/18/1998 | NEVA SYSTEM | UROMETRICS, INC. |
| DEN000006 | 04/27/2000 | EROS-CLITORAL THERAPY DEVICE (CTD) | UROMETRICS, INC. |
| K971790 | 05/14/1997 | KNOLL/MIDUS (MALE IMPOTENCE DIAGNOSTIC ULTRASONIC SYSTEM) | UROMETRICS, INC. |
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