Medical Device Manufacturer · US , South West Ranches , FL

Visiomed AG - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2004

Recent clearances: MICRODERM, MODEL/VERSION 3.5

View 1 510(k) Devices ↓

1

Total

1

Cleared

0

Denied

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

1 devices

1-1 of 1

Cleared Jun 08, 2004

MICRODERM, MODEL/VERSION 3.5

General & Plastic Surgery · 134d