Palomar Medical Products, Inc. - FDA 510(k) Cleared Devices
Recent clearances: EMERGE FRACTIONAL LASER, MODIFICATION TO LUX1540 HANDPIECE AND LUX 1440 HANDPIECE, THERMAPULSE
21
Total
21
Cleared
0
Denied
FDA 510(k) Regulatory Record - Palomar Medical Products, Inc. Physical Medicine ✕
2 devices