
Well-Life Healthcare, Inc.
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LIMITED FUNCTION WL/OTC-TENS DEVICE, MODEL WL-2103A, WL-2203A, WL-2203B AND WL-2401 is an FDA 510(k)-cleared medical device (K040512) manufactured by Well-Life Healthcare, 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 May 26, 2004. Regulation: 8.