VISTA MR 2055 HP SYSTEM AND 2055 UPGRADES

VISTA MR 2055 HP SYSTEM AND 2055 UPGRADES is an FDA 510(k)-cleared medical device (K893739) 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 July 13, 1989. Regulation: 8.