VersaCross? RF Wire
Nov 2024
108d
Baylis Medical Company
1
Total
1
Cleared
0
Denied
Baylis Medical Company — FDA 510(k) Submissions
Baylis Medical Company 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, Septostomy . Use the specialty filter in the sidebar to narrow results.
1 devices