
C.R. Bard, Inc.
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TRIFUSION, MODEL 0609190/0659350 is an FDA 510(k)-cleared medical device (K041088) manufactured by C.R. Bard, 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 31, 2004. Regulation: 8.

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