North American Philips Corp. - FDA 510(k) Cleared Devices

North American Philips Corp. has 14 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 14 cleared submissions from 1981 to 1984. Primary specialty: Cardiovascular.

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