Perahealth, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Perahealth, Inc. - FDA 510(k) Cleared Devices
Recent clearances: PeraMobile and PeraWatch, PeraServer and PeraTrend
2
Total
2
Cleared
0
Denied
Perahealth, Inc. has 2 FDA 510(k) cleared medical devices. Based in Charlotte, US.
Historical record: 2 cleared submissions from 2018 to 2019. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Perahealth, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Biologics Consulting and Biologics Consulting Group.
FDA 510(k) Regulatory Record - Perahealth, Inc.
2 devices