Dr. K. Honle GmbH
FDA 510(k) & PMA Approved Devices — 3 products
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Total Devices3
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K828676 | DERMALIGHT SPOT | 1983-01-17 | View | |
| 510(k) | K828674 | DERMALIGHT BLUE-POINT | 1983-01-17 | View | |
| 510(k) | K828675 | DERMALIGHT UVASTAR 400 | 1983-01-17 | View |
No matching devices.
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