INTERLINK MICRO-INFUSION MANIFOLD EXTENSION SETS

INTERLINK MICRO-INFUSION MANIFOLD EXTENSION SETS is an FDA 510(k)-cleared medical device (K970438) 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 April 1, 1997. Regulation: 8.