
Arrow Intl., Inc.
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AC 3 LUMEN CENTRAL VENOUS ACCESS KIT WITH ARROWG+ARD ANTIMICROBIAL SURFACE is an FDA 510(k)-cleared medical device (K032962) manufactured by Arrow Intl., 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 October 28, 2003. Regulation: 8.

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