Medical Device Manufacturer · US , Oklahoma City , OK

Clay Kennard - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2006

Total

Cleared

Denied

Clay Kennard has 1 FDA 510(k) cleared medical devices. Based in Oklahoma City, US.

Historical record: 1 cleared submissions from 2006 to 2006. Primary specialty: Gastroenterology & Urology.

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

Clay Kennard 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 - Clay Kennard

1 devices

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