BEACON-P, MODEL 211059

BEACON-P, MODEL 211059 is an FDA 510(k)-cleared medical device (K992335) 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 October 6, 1999. Regulation: 8.