MODEL 2031 TMJ SURFACE COIL

MODEL 2031 TMJ SURFACE COIL is an FDA 510(k)-cleared medical device (K895131) manufactured by Medical Advances, 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 26, 1989. Regulation: 8.