HEAD COIL GEOMETRIC DISTOR SPEC FOR VISTA HPQ SYST

HEAD COIL GEOMETRIC DISTOR SPEC FOR VISTA HPQ SYST is an FDA 510(k)-cleared medical device (K920199) 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 5, 1992. Regulation: 8.