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ElectroCore Files FDA Submission For Quell In Persistent Chemotherapy-Related Neuropathy; Stock Up
Source: Nasdaq
Healthcare & BiotechRegulation & LegislationProduct Launches
electroCore, Inc. submitted a 510(k) premarket notification to the U.S. FDA seeking clearance for its Quell wearable neuromodulation platform. The article excerpt does not report an FDA decision or provide further details on the intended treatment indication.
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