InnoCare Specialty Foley Catheter
Sep 2024
121d
Innocare Urologics, LLC
1
Total
1
Cleared
0
Denied
Innocare Urologics, LLC — FDA 510(k) Submissions
Innocare Urologics, LLC has submitted 1 FDA 510(k) premarket notifications since 2024, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Catheter, Retention Type, Balloon . Use the specialty filter in the sidebar to narrow results.
1 devices