MiniCollect K2E K2EDTA Tubes

MiniCollect K2E K2EDTA Tubes is an FDA 510(k)-cleared medical device (K182078) manufactured by Greiner Bio-One Na, Inc.. This device is classified under the Clinical Chemistry specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 24, 2019. Regulation: 8.