hygh-tec Drainage II
Jan 2025
163d
Amb Medtec
1
Total
1
Cleared
0
Denied
Amb Medtec — FDA 510(k) Submissions
Amb Medtec has submitted 1 FDA 510(k) premarket notifications since 2025, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Tubes, Gastrointestinal (and Accessories) . Use the specialty filter in the sidebar to narrow results.
1 devices