Lynton Lasers Limited - FDA 510(k) Cleared Devices
Recent clearances: LUMACARE MODEL LC-122M NON-COHERENT LIGHT SOURCE AND MODEL LUM-P FIBRE OPTIC PROBE, LUMINA INTENSE PULSED LIGHT (& LASER) SYSTEM, LUMACARE LC-122M NON-COHERENT LIGHT SOURCE
3
Total
3
Cleared
0
Denied