Medical Device Manufacturer · US , Redmond , WA

Spiration, Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2015

Total

Cleared

Denied

Spiration, Inc. has 5 FDA 510(k) cleared medical devices. Based in Redmond, US.

Historical record: 5 cleared submissions from 2015 to 2017. Primary specialty: Ear, Nose, Throat.

Browse the FDA 510(k) cleared devices submitted by Spiration, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Spiration, Inc.

5 devices

1-5 of 5