Medical Device Manufacturer · US , Pasadena , CA

Gi Logic, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2015

Total

Cleared

Denied

Gi Logic, Inc. has 1 FDA 510(k) cleared medical devices. Based in Pasadena, US.

Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: Cardiovascular.

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

Gi Logic, Inc. is one of 4878 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Gi Logic, Inc.

1 devices

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