TECH DYNE - HP-2000, SKREEN TEST, RMS-200

TECH DYNE - HP-2000, SKREEN TEST, RMS-200 is an FDA 510(k)-cleared medical device (K920183) manufactured by Tech Dyne Group. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 14, 1992. Regulation: 8.