
Vasocor, Inc.
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VASOCOR VASCULAR DIAGNOSTIC CENTER (MODEL 300) is an FDA 510(k)-cleared medical device (K011625) manufactured by Vasocor, 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 January 22, 2002. Regulation: 8.