IPUMP PAIN MANAGEMENT SYSTEM, MODEL 2L3107, 2L3107K

IPUMP PAIN MANAGEMENT SYSTEM, MODEL 2L3107, 2L3107K is an FDA 510(k)-cleared medical device (K052973) 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 January 24, 2007. Regulation: 8.