PRO-LOCK(TM) SHIELDING NEEDLE CONNECTOR ASSEMBLY

PRO-LOCK(TM) SHIELDING NEEDLE CONNECTOR ASSEMBLY is an FDA 510(k)-cleared medical device (K901081) manufactured by Vlv Associates, 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 June 7, 1990. Regulation: 8.