Medical Device Manufacturer · US , Palo Alto , CA

Cognoa, Inc.

2 submissions · 1 cleared · Since 2021
2
Total
1
Cleared
1
Denied

Cognoa, Inc. — FDA 510(k) Submissions

Cognoa, Inc. has submitted 2 FDA 510(k) premarket notifications since 2021, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Pediatric Autism Spectrum Disorder Diagnosis Aid . Use the specialty filter in the sidebar to narrow results.

2 devices
1–2 of 2
Filters
Filter by Specialty
All2 Neurology 2