Medical Device Manufacturer · US , Cary , NC

Palomar - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2001
Official Website
2
Total
2
Cleared
0
Denied

FDA 510(k) Regulatory Record - Palomar General & Plastic Surgery ✕

2 devices
1-2 of 2
Cleared Jun 19, 2002
PALOMAR LUXG HANDPIECE
K020941 · GEX
General & Plastic Surgery · 89d
Cleared Sep 10, 2001
PALOMAR DERMALUX PULSED LIGHT SYSTEM
K010618 · GEX
General & Plastic Surgery · 193d
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