PHILIPS ANGIOPRO RELEASE 2.1

PHILIPS ANGIOPRO RELEASE 2.1 is an FDA 510(k)-cleared medical device (K933791) 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 November 21, 1993. Regulation: 8.