Epiep, Inc. is one of 18443 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Epiep, Inc. - FDA 510(k) Cleared Devices
Recent clearances: EpiAccess System, EpiAccess System
2
Total
2
Cleared
0
Denied
Epiep, Inc. has 2 FDA 510(k) cleared medical devices. Based in New Haven, US.
Historical record: 2 cleared submissions from 2014 to 2017. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Epiep, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Cygnus Regulatory as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Epiep, Inc.
2 devices