FDA 510(k), K071822, URGENT PC NEUROMODULATION SYSTEM, MODELS UPC200 AND UPC250-12

FDA 510(k), K071822, URGENT PC NEUROMODULATION SYSTEM, MODELS UPC200 AND UPC250-12

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510(K) Number: K071822
Device Name: URGENT PC NEUROMODULATION SYSTEM, MODELS UPC200 AND UPC250-12
Manufacturer: UROPLASTY, INC.
Device Classification Name: stimulator, peripheral nerve, non-implanted, for urinary incontinence
Regulation Number: 876.5310
Classification Product Code: NAM
Date Received: 07/03/2007
Decision Date: 08/20/2007
Regulation Medical Specialty: Gastroenterology/Urology

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