
Medical Cv, Inc.
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NORTHRUP UNIVERSAL ANNULOPLASTY SYSTEM, MODEL 1000 is an FDA 510(k)-cleared medical device (K033685) manufactured by Medical Cv, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 2, 2004. Regulation: 8.