
Becton Dickinson Vascular Access, Inc.
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INSYTE INTRODUCER CATHETER is an FDA 510(k)-cleared medical device (K942045) manufactured by Becton Dickinson Vascular Access, 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 January 8, 1995. Regulation: 8.

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