
Heraeus Kulzer, Inc.
Free shipping on orders over $99 · 30-day returns
TECHNICON H* 3 RTX SYSTEM (IN-VITRO DIAG. SYSTEM) is an FDA 510(k)-cleared medical device (K930148) manufactured by Heraeus Kulzer, 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 May 10, 1993. Regulation: 8.