Medical Device Manufacturer · US , Minneapolis , MN

Crosstex International - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2008

Total

Cleared

Denied

Crosstex International has 4 FDA 510(k) cleared medical devices. Based in Minneapolis, US.

Historical record: 4 cleared submissions from 2008 to 2014. Primary specialty: General Hospital.

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

Crosstex International is one of 5103 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

Crosstex International — FDA 510(k) Products and Clearance History

4 devices

1-4 of 4