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.

Inrange Systems, Inc. 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 - Inrange Systems, Inc.

2 devices

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