George H. Frisch
FDA 510(k) & PMA Approved Devices — 2 products
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Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K803121 | MENTOR 150 TRANSCUTANEOUS NERVE STIMULA | GZJ | 1980-12-30 | View |
| 510(k) | K803113 | MENTOR 402 TRANSCUTANEOUS ELEC. STIMULAT | GZJ | 1980-12-30 | View |
No matching devices.
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