
Pro-Med Instruments GmbH
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DORO RADIOLUCENT HEADREST SYSTEM ( ALSO MRI-COMPATIBLE) AND COMPONENTS is an FDA 510(k)-cleared medical device (K063494) manufactured by Pro-Med Instruments GmbH. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 20, 2007. Regulation: 8.