Q-Pad Test System
Dec 2023
201d
Qurasense
1
Total
1
Cleared
0
Denied
Qurasense — FDA 510(k) Submissions
Qurasense has submitted 1 FDA 510(k) premarket notifications since 2023, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Assay, Glycosylated Hemoglobin . Use the specialty filter in the sidebar to narrow results.
1 devices