SYNCRA TILT OPTION FOR ANGIO DIAGNOST 5

SYNCRA TILT OPTION FOR ANGIO DIAGNOST 5 is an FDA 510(k)-cleared medical device (K940696) manufactured by Philips Medical Systems North America, 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 15, 1994. Regulation: 8.