Medical Device Manufacturer · SE , Bulach

Schneider (Europe) GmbH - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1995
5
Total
5
Cleared
0
Denied

FDA 510(k) Regulatory Record - Schneider (Europe) GmbH Gastroenterology & Urology

1 devices
1-1 of 1
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