INTERLINK ADAPTER FOR CONVENTIONAL Y-SITE

INTERLINK ADAPTER FOR CONVENTIONAL Y-SITE is an FDA 510(k)-cleared medical device (K962893) manufactured by Baxter Healthcare Corp. 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 October 17, 1996. Regulation: 8.