ENFit to ENFit Extension Sets
Nov 2023
269d
Vesco Medical
1
Total
1
Cleared
0
Denied
Vesco Medical — FDA 510(k) Submissions
Vesco Medical 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 Gastrointestinal Tubes With Enteral Specific Connectors . Use the specialty filter in the sidebar to narrow results.
1 devices