Medical Device Manufacturer · US , South St. Paul , MN

Verilux - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2010

1

Total

1

Cleared

0

Denied

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

1 devices

1-1 of 1

Cleared Sep 03, 2010

CLEARWAVE PHOTOTHERAPY SYSTEM FOR ACNE, MODEL: CWST2

General & Plastic Surgery · 504d