Peel-Away Introducer Sheath
Feb 2026
42d
VascuTech Medical, LLC
1
Total
1
Cleared
0
Denied
VascuTech Medical, LLC — FDA 510(k) Submissions
VascuTech Medical, 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 Introducer, Catheter . Use the specialty filter in the sidebar to narrow results.
1 devices