Shift Labs is one of 19883 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
1
Total
1
Cleared
0
Denied
Shift Labs has 1 FDA 510(k) cleared medical devices. Based in Seattle, US.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Shift Labs Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Drug and Device Development Co., Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Shift Labs
1 devices