Medical Device Manufacturer · US , Crescent Springs , KY

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

1 submissions · 1 cleared · Since 2018

Total

Cleared

Denied

Kdb Inc. (Dba) Sperti Sunlamp has 1 FDA 510(k) cleared medical devices. Based in Crescent Springs, US.

Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Kdb Inc. (Dba) Sperti Sunlamp Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Kdb Inc. (Dba) Sperti Sunlamp

1 devices

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