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FDA Granted 510(K) Clearances to Hollywog's New Witouch and Witouch Pro Wireless
Dec 5, 2012The US Food and Drug Administration (FDA) has granted 510(k) clearances to Hollywog's new WiTouch and WiTouch Pro wireless remote controlled devices. The WiTouch devices, which incorporates TENS technology, are designed for the ...
Tags: FDA, treatment of back pain, wireless remote controlled device
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