Medical Device Manufacturer · US , Pleasanton , CA

Interson Corporation - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2017

Total

Cleared

Denied

Interson Corporation has 2 FDA 510(k) cleared medical devices. Based in Pleasanton, US.

Last cleared in 2023. Active since 2017. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Interson Corporation Filter by specialty or product code using the sidebar.

Interson Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Interson Corporation

2 devices

1-2 of 2