Medical Device Manufacturer · SE , Uppsala

Circassia AB

1 submissions · 1 cleared · Since 2017
1
Total
1
Cleared
0
Denied

Circassia AB — FDA 510(k) Submissions

Circassia AB has submitted 1 FDA 510(k) premarket notifications since 2017, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include System, Test, Breath Nitric Oxide . Use the specialty filter in the sidebar to narrow results.

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