M3290B Philips IntelliVue Information Center iX

M3290B Philips IntelliVue Information Center iX is an FDA 510(k)-cleared medical device (K163584) manufactured by Philips Medical Systems. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 6, 2017. Regulation: 8.