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

Verilux - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2010

Recent clearances: CLEARWAVE PHOTOTHERAPY SYSTEM FOR ACNE, MODEL: CWST2

1
Total
1
Cleared
0
Denied

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

1 devices
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