CFP-3131, CFP-2222

CFP-3131, CFP-2222 is an FDA 510(k)-cleared medical device (K201172) manufactured by Mx Imaging, 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 May 28, 2020. Regulation: 8.