CELLECT MODEL D, AUTOMATED HEMTALOGY ANALYZER

CELLECT MODEL D, AUTOMATED HEMTALOGY ANALYZER is an FDA 510(k)-cleared medical device (K874763) manufactured by Instrumentation Laboratory CO. This device is classified under the Hematology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 17, 1988. Regulation: 8.