Santreva?-ATK Endovascular Revasculariztion Catheter
Sep 2025
59d
AngioSafe, Inc.
1
Total
1
Cleared
0
Denied
AngioSafe, Inc. — FDA 510(k) Submissions
AngioSafe, Inc. 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 Catheter For Crossing Total Occlusions . Use the specialty filter in the sidebar to narrow results.
1 devices