Medical Device Manufacturer · US , Seattle , WA

Shift Labs, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2018

Total

Cleared

Denied

Shift Labs, Inc. has 1 FDA 510(k) cleared medical devices. Based in Seattle, US.

Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: General Hospital.

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

1 devices

1–1 of 1