3M CDI H/S CUVETTES WITH HEPARON TREATMENT

3M CDI H/S CUVETTES WITH HEPARON TREATMENT is an FDA 510(k)-cleared medical device (K973472) manufactured by 3M Healthcare. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 7, 1997. Regulation: 8.