Lynton Lasers Limited
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) | K072048 | LUMACARE MODEL LC-122M NON-COHERENT LIGHT SOURCE AND MODEL LUM-P FIBRE OPTIC PROBE | ILY | 2007-11-16 | View |
| 510(k) | K063427 | LUMINA INTENSE PULSED LIGHT (& LASER) SYSTEM | GEX | 2007-07-25 | View |
| 510(k) | K062871 | LUMACARE LC-122M NON-COHERENT LIGHT SOURCE | GEX | 2006-11-14 | View |
No matching devices.
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