
Arrow International, Inc. (Subsidiary of Teleflex
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CG+ Arrow JACC is an FDA 510(k)-cleared medical device (K161765) manufactured by Arrow International, Inc. (Subsidiary of Teleflex. 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 September 5, 2016. Regulation: 8.

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