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www.fdanews.com/articles/149065-zynex-obtains-fda-510-k-clearance-for-inwave-medical-device

Zynex Obtains FDA 510(k) Clearance for InWave Medical Device

August 30, 2012
Zynex, a provider and developer of non-invasive medical devices for electrotherapy, stroke rehabilitation, neurological diagnosis and cardiac monitoring, announced that it received FDA 510(k) clearance on its InWave medical device.
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