Light Force Therapy, 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) | K022888 | ACUBEAM, SUPER NOVA, DIO | ILY | 2002-12-11 | View |
| 510(k) | K001179 | SUPER NOVA, ACUBEAM | ILY | 2000-10-27 | View |
No matching devices.
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