Medical Device Manufacturer · US , Pensacola , FL

Actigraph - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2018

Recent clearances: ActiGraph CentrePoint Insight Watch

View 1 510(k) Devices ↓

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Actigraph Neurology ✕

1 devices

1-1 of 1

Cleared May 24, 2018

ActiGraph CentrePoint Insight Watch

Neurology · 30d