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Bioject, Inc.
Free shipping on orders over $99 · 30-day returns
RECONSTITUTION KIT & VIAL CONNECTOR is an FDA 510(k)-cleared medical device (K010623) manufactured by Bioject, 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 April 4, 2001. Regulation: 8.

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