Xltek is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Xltek - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Xltek has 3 FDA 510(k) cleared medical devices. Based in Oakville, CA.
Historical record: 3 cleared submissions from 2000 to 2002. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Xltek Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Xltek
3 devices