Medical Device Manufacturer · US , Fr. Myers , FL

Sintea Plustek - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2014

Total

Cleared

Denied

Sintea Plustek has 1 FDA 510(k) cleared medical devices. Based in Fr. Myers, US.

Historical record: 1 cleared submissions from 2014 to 2014. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Sintea Plustek Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Sintea Plustek

1 devices

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