Medical Device Manufacturer · SE , Gothenburg, Askim

Oticon Medical AB - FDA 510(k) Cleared Devices

16 submissions · 16 cleared · Since 2008
16
Total
16
Cleared
0
Denied
FDA 510(k) Regulatory Record - Oticon Medical AB General Hospital ✕
1 devices
1-1 of 1
Cleared Sep 23, 2014
STERILIZATION CASSETTE
K141616 · KCT
General Hospital · 99d
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