ANGIOCATH(R) NONVALON(R) AND ANGIO-SET(R) IV CATHETERS

ANGIOCATH(R) NONVALON(R) AND ANGIO-SET(R) IV CATHETERS is an FDA 510(k)-cleared medical device (K950301) 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 April 17, 1995. Regulation: 8.