Vitaphore Corp. - FDA 510(k) Cleared Devices

Vitaphore Corp. has 12 FDA 510(k) cleared medical devices. Based in San Francisco, US.

Historical record: 12 cleared submissions from 1986 to 1992. Primary specialty: General Hospital.

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