Medical Device Manufacturer · US , Broomall , PA

Vestibular First

1 submissions · 1 cleared · Since 2020
1
Total
1
Cleared
0
Denied

Vestibular First — FDA 510(k) Submissions

Vestibular First has submitted 1 FDA 510(k) premarket notifications since 2020, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Nystagmograph . Use the specialty filter in the sidebar to narrow results.

1 devices
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All1 Ear, Nose, Throat 1