PERSONAL INFUSOR LOCAL PAIN MANAGEMENT PROCEDURAL KIT

PERSONAL INFUSOR LOCAL PAIN MANAGEMENT PROCEDURAL KIT is an FDA 510(k)-cleared medical device (K010824) manufactured by Science Incorporated. 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 June 4, 2001. Regulation: 8.