MAG RESON DIAG DEV ACCESS SPEC PURP REC ONLY COIL

MAG RESON DIAG DEV ACCESS SPEC PURP REC ONLY COIL is an FDA 510(k)-cleared medical device (K901952) manufactured by Siemens Medical Solutions USA, 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 August 16, 1990. Regulation: 8.