VISTA HPQ SYSTEM, VISTA MR 2055 HP SYSTEM

VISTA HPQ SYSTEM, VISTA MR 2055 HP SYSTEM is an FDA 510(k)-cleared medical device (K900064) manufactured by Philips Medical Systems (Cleveland), Inc.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 8, 1990. Regulation: 8.