Medical Device Manufacturer · US , Oklahoma City , OK

Corazonix Corp. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1987

Total

Cleared

Denied

Corazonix Corp. has 2 FDA 510(k) cleared medical devices. Based in Oklahoma City, US.

Historical record: 2 cleared submissions from 1987 to 1988. Primary specialty: Cardiovascular.

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

Corazonix Corp. 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 - Corazonix Corp.

2 devices

1-2 of 2