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Medrad, Inc.
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO MEDRAD CONTINUUM MR INFUSION SYSTEM is an FDA 510(k)-cleared medical device (K061128) manufactured by Medrad, Inc.. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 21, 2006. Regulation: 8.

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