Medical Device Manufacturer · US , New Haven , CT

Epiep, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2014

Total

Cleared

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.

Epiep, Inc. is one of 4719 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Epiep, Inc.

2 devices

1-2 of 2