Urometrics, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
Advertisement
Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K980627 | NEVA SYSTEM | LIL | 1998-04-07 | View |
| 510(k) | K971790 | KNOLL/MIDUS (MALE IMPOTENCE DIAGNOSTIC ULTRASONIC SYSTEM) | IYN | 1997-12-17 | View |
No matching devices.
Advertisement