
Medical Device Consultants, Inc.
Free shipping on orders over $99 · 30-day returns
ADDITIONAL HEMOTEC ACT COAGULATION CARTRIDGES is an FDA 510(k)-cleared medical device (K853198) manufactured by Medical Device Consultants, Inc.. This device is classified under the Hematology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 3, 1985. Regulation: 8.