Medical Device Manufacturer · US , Altoona , PA

Inrange Systems, Inc. - FDA 510(k) Cleared Devices

2 submissions · 1 cleared · Since 2007

Total

Cleared

Denied

Inrange Systems, Inc. has 1 FDA 510(k) cleared medical devices. Based in Altoona, US.

Historical record: 1 cleared submissions from 2007 to 2015. Primary specialty: General Hospital.

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

FDA 510(k) Regulatory Record - Inrange Systems, Inc.

2 devices

1-2 of 2