PeriCALM Patterns 3.0
Jan 2025
273d
Perigen, Inc.
1
Total
1
Cleared
0
Denied
Perigen, Inc. — FDA 510(k) Submissions
Perigen, 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 System, Monitoring, Perinatal . Use the specialty filter in the sidebar to narrow results.
1 devices