inui In-Home Urine Analysis Test System
May 2018
106d
Scanadu, Inc.
1
Total
1
Cleared
0
Denied
Scanadu, Inc. — FDA 510(k) Submissions
Scanadu, Inc. has submitted 1 FDA 510(k) premarket notifications since 2018, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Method, Enzymatic, Glucose (urinary, Non-quantitative) . Use the specialty filter in the sidebar to narrow results.
1 devices