Pulse Biosciences Announces FDA IDE Approval and Initiation of Sebaceous Hyperplasia Study

Pulse Biosciences Announces FDA IDE Approval and Initiation of Sebaceous Hyperplasia Study

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HAYWARD, Calif.--(BUSINESS WIRE)--Pulse Biosciences, Inc. (Nasdaq: PLSE), a novel bioelectric medicine company progressing Nano-Pulse Stimulation™ (NPS™) technology, today announced FDA Investigational Device Exemption (IDE) approval and initiation of a pivotal study to evaluate the treatment of sebaceous hyperplasia (SH) lesions using the CellFX® System. The data generated from this study is intended to support a 510(k) submission to expand the indication for use of the CellFX System specifica

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