Medical Device Manufacturer · US , Wilmington , DE

Isag Rx, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2017

Total

Cleared

Denied

Isag Rx, Inc. has 1 FDA 510(k) cleared medical devices. Based in Wilmington, US.

Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: General Hospital.

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

Isag Rx, Inc. is one of 4730 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Isag Rx, Inc.

1 devices

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