Medical Device Manufacturer · US , Pensacola , FL

Actigraph - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2018

Total

Cleared

Denied

Actigraph has 1 FDA 510(k) cleared medical devices. Based in Pensacola, US.

Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: Neurology.

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FDA 510(k) Regulatory Record - Actigraph

1 devices

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