
Becton Dickinson Vascular Access, Inc.
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INSYTE SIDEHOLDED DRAINAGE CATHETER is an FDA 510(k)-cleared medical device (K950439) manufactured by Becton Dickinson Vascular Access, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on March 13, 1995. Regulation: 8.