Vitaid, Ltd. - FDA 510(k) Cleared Devices

Vitaid, Ltd. has 7 FDA 510(k) cleared medical devices. Based in Ontario, Canada, CA.

Historical record: 7 cleared submissions from 1989 to 2005. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Vitaid, Ltd. Filter by specialty or product code using the sidebar.