CDI(TM) 300, 400 & 100, MODIFICATION

CDI(TM) 300, 400 & 100, MODIFICATION is an FDA 510(k)-cleared medical device (K915255) manufactured by 3M Company. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 14, 1992. Regulation: 8.