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NeuroMetrix completes 510(k) clearance process for SENSUS device

NeuroMetrix reported that it has received 510(k) clearance from the U.S. Food and Drug Administration for the disposable electrode that is used in conjunction with its SENSUS device. This regulatory determination by the FDA gives NeuroMetrix clearance to market the SENSUS Pain Management System in the U.S. market, the company said.