CDI(TM) H/S CUVETTE, MODIFICATION

CDI(TM) H/S CUVETTE, MODIFICATION is an FDA 510(k)-cleared medical device (K915265) 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.