Medical Device Manufacturer · US , San Jose , CA

Spirair, Inc.

4 submissions · 4 cleared · Since 2023
4
Total
4
Cleared
0
Denied

Spirair, Inc. — FDA 510(k) Submissions

Spirair, Inc. has submitted 4 FDA 510(k) premarket notifications since 2023, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Polymer, Ear, Nose And Throat, Synthetic, Absorbable, Splint, Intranasal Septal . Use the specialty filter in the sidebar to narrow results.

4 devices
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All4 Ear, Nose, Throat 4