MULTI PURPOSE FLEX ARRAY COIL : MODEL 235 SERIES

MULTI PURPOSE FLEX ARRAY COIL : MODEL 235 SERIES is an FDA 510(k)-cleared medical device (K000345) 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 April 10, 2000. Regulation: 8.