MX MOBILE X-RAY SYSTEM

MX MOBILE X-RAY SYSTEM is an FDA 510(k)-cleared medical device (K862452) 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 21, 1986. Regulation: 8.