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Theratech, Inc.
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IF TRUE SINE INTERFERENTIAL STIMULATOR, MODEL WL-2206A is an FDA 510(k)-cleared medical device (K050847) manufactured by Theratech, 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 June 16, 2005. Regulation: 8.