Medical Device Manufacturer · US , Pensacola , FL

Actigraph, LLC

2 submissions · 2 cleared · Since 2008
2
Total
2
Cleared
0
Denied

Actigraph, LLC — FDA 510(k) Submissions

Actigraph, LLC has submitted 2 FDA 510(k) premarket notifications since 2008, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Exerciser, Measuring, Device, Sleep Assessment . Use the specialty filter in the sidebar to narrow results.

2 devices
1–2 of 2
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All2 Physical Medicine 1 Neurology 1