Medical Device Manufacturer · US , Cary , NC

Palomar - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2001

Recent clearances: PALOMAR LUXG HANDPIECE, PALOMAR DERMALUX PULSED LIGHT SYSTEM

View 2 510(k) Devices ↓ 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

General & Plastic Surgery · 89d

Cleared Sep 10, 2001

PALOMAR DERMALUX PULSED LIGHT SYSTEM

General & Plastic Surgery · 193d