Promatek Industries, Ltd. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Promatek Industries, Ltd. - FDA 510(k) Cleared Devices
3
Total
2
Cleared
0
Denied
Promatek Industries, Ltd. has 2 FDA 510(k) cleared medical devices. Based in Quebec, H4p 2c9, CA.
Historical record: 2 cleared submissions from 1987 to 1990. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Promatek Industries, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Promatek Industries, Ltd.
3 devices