Crosstex International, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Crosstex International, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Crosstex International, Inc. has 2 FDA 510(k) cleared medical devices. Based in Minneapolis, US.
Historical record: 2 cleared submissions from 2010 to 2011. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Crosstex International, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Crosstex International, Inc.
2 devices