Medical Device Manufacturer · US , Washington , DC

Cortex Technology Aps - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1998

Total

Cleared

Denied

Cortex Technology Aps has 2 FDA 510(k) cleared medical devices. Based in Washington, US.

Historical record: 2 cleared submissions from 1998 to 1999. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Cortex Technology Aps Filter by specialty or product code using the sidebar.

Cortex Technology Aps is one of 9722 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Cortex Technology Aps

2 devices

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