Medical Device Manufacturer · US , Worchester , MA

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

4 submissions · 3 cleared · Since 2017

Total

Cleared

Denied

Interscope, Inc. has 3 FDA 510(k) cleared medical devices. Based in Worchester, US.

Historical record: 3 cleared submissions from 2017 to 2019. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by Interscope, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Interscope, Inc.

4 devices

1-4 of 4