Medical Device Manufacturer · DE , Zeulenroda-Triebes

Bauerfeind AG - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2011

Recent clearances: BODYTRONIC 200, VENOTRAIN CURAFLOW

View 2 510(k) Devices ↓ Official Website

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Bauerfeind AG General Hospital ✕

1 devices

1-1 of 1

Cleared Oct 04, 2011

VENOTRAIN CURAFLOW

General Hospital · 112d