Medical Device Manufacturer · US , Menlo Park , CA

Crux Biomedical - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2012

Total

Cleared

Denied

Crux Biomedical has 2 FDA 510(k) cleared medical devices. Based in Menlo Park, US.

Historical record: 2 cleared submissions from 2012 to 2013. Primary specialty: Cardiovascular.

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

Crux Biomedical is one of 5703 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Crux Biomedical

2 devices

1-2 of 2