EPIDURAL INDICATION FOR BAXTER SYRINGE INFUS PUMP

EPIDURAL INDICATION FOR BAXTER SYRINGE INFUS PUMP is an FDA 510(k)-cleared medical device (K911289) 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 May 20, 1991. Regulation: 8.