Webest Multi-Drug Urine Cup; Webest Home Multi-Drug Urine Cup
Mar 2026
34d
WEBEST Biotech,, LLC
1
Total
1
Cleared
0
Denied
WEBEST Biotech,, LLC — FDA 510(k) Submissions
WEBEST Biotech,, LLC has submitted 1 FDA 510(k) premarket notifications since 2026, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Test, Amphetamine, Over The Counter . Use the specialty filter in the sidebar to narrow results.
1 devices