FDA 510(k), K182581, PlayMakar Sport Muscle Stimulator, Model PRO-500

FDA 510(k), K182581, PlayMakar Sport Muscle Stimulator, Model PRO-500

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510(K) Number: K182581
Device Name: PlayMakar Sport Muscle Stimulator, Model PRO-500
Manufacturer: Mike Williams
Device Classification Name: Stimulator, Nerve, Transcutaneous, Over-The-Counter
Regulation Number: NUH
Classification Product Code: 09/19/2018
Date Received: 11/21/2018
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Neurology

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