AEROQUIP SAFESTART IV CATHETER

AEROQUIP SAFESTART IV CATHETER is an FDA 510(k)-cleared medical device (K970669) manufactured by Aeroquip Medical Products. 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 July 31, 1997. Regulation: 8.