Medical Device Manufacturer · US , Crescent Springs , KY

Kdb Inc. (Dba) Sperti Sunlamp - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2018
1
Total
1
Cleared
0
Denied

FDA 510(k) Regulatory Record - Kdb Inc. (Dba) Sperti Sunlamp General & Plastic Surgery

1 devices
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