
Western Clinical Technology Systems, Inc.
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ECHOPULSE MUSCLE STIMULATOR SYSTEM, MODEL 800 is an FDA 510(k)-cleared medical device (K023230) manufactured by Western Clinical Technology 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 May 4, 2003. Regulation: 8.