
Vectracor, Inc.
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VECTRAPLEXECG SYSTEM WITH VECTRAPLEXAMI is an FDA 510(k)-cleared medical device (K102378) manufactured by Vectracor, 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 November 1, 2011. Regulation: 8.