Medical Device Manufacturer · US , Bartlett , TN

Scanditronix Wellhofer North America - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2000

Total

Cleared

Denied

Scanditronix Wellhofer North America has 1 FDA 510(k) cleared medical devices. Based in Bartlett, US.

Historical record: 1 cleared submissions from 2000 to 2000. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Scanditronix Wellhofer North America Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Scanditronix Wellhofer North America

1 devices

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