Theramed, Inc.
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) | K910004 | FURUI SHUNT, 2-WAY AND 3-WAY | DWF | 1991-09-19 | View |
| 510(k) | K895524 | HYDROCEPHALUS SHUNT SYSTEM, LOW/MEDIUM/HIGH PRESS. | JXG | 1990-04-10 | View |
No matching devices.
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