Surgilight, 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) | K020973 | EX-308 EXCIMER LASER FOR PHOTOTHERAPY TREATMENT OF VITILIGO | GEX | 2002-03-29 | View |
| 510(k) | K993328 | SURGILIGHT, INC EXCIMER LASER | GEX | 2000-07-18 | View |
No matching devices.
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