MLS ELECTROMYOGRAPHIC PREAMPLIFIER

MLS ELECTROMYOGRAPHIC PREAMPLIFIER is an FDA 510(k)-cleared medical device (K974385) manufactured by Motion Lab Systems, Inc.. This device is classified under the Physical Medicine specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 18, 1998. Regulation: 8.