Medical Device Manufacturer · DE , Zeulenroda-Triebes

Bauerfeind AG - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2011
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
K111662 · DWL
General Hospital · 112d
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