EPIDURAL INDICATION FOR BAXTER INFUSORS ATTACHMENT

EPIDURAL INDICATION FOR BAXTER INFUSORS ATTACHMENT is an FDA 510(k)-cleared medical device (K905778) 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 July 11, 1991. Regulation: 8.