
Myotronics-Noromed, Inc.
Free shipping on orders over $99 · 30-day returns
MODEL MES-9000/EMG SYSTEM is an FDA 510(k)-cleared medical device (K013399) manufactured by Myotronics-Noromed, Inc.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 12, 2001. Regulation: 8.