Medical Device Manufacturer · CH , Zurich

Comerge AG - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2024

Recent clearances: T1D1, Neo ADVISE software

2
Total
2
Cleared
0
Denied

FDA 510(k) Regulatory Record - Comerge AG Orthopedic

1 devices
1-1 of 1
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