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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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