Vivo 45 LS
Dec 2025
865d
Oconnell Regulatory Consultants, Inc.
1
Total
1
Cleared
0
Denied
Oconnell Regulatory Consultants, Inc. — FDA 510(k) Submissions
Oconnell Regulatory Consultants, 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 Ventilator, Continuous, Facility Use . Use the specialty filter in the sidebar to narrow results.
1 devices