INFUSAFE 205 CATOLOG NO. 205.000

INFUSAFE 205 CATOLOG NO. 205.000 is an FDA 510(k)-cleared medical device (K852433) manufactured by Medix Medical Electronics (U.S.A.), Inc.. 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 26, 1985. Regulation: 8.