ENDOHELIX ENDARTERECTOMY DEVICE
Oct 2003
114d
Endarx, Inc.
1
Total
1
Cleared
0
Denied
Endarx, Inc. — FDA 510(k) Submissions
Endarx, Inc. has submitted 1 FDA 510(k) premarket notifications since 2003, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Stripper, Artery, Intraluminal . Use the specialty filter in the sidebar to narrow results.
1 devices