FDA 510(k), K130368, AUTOLITH TOUCH; URO TOUCH

FDA 510(k), K130368, AUTOLITH TOUCH; URO TOUCH

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510(K) Number: K130368
Device Name: AUTOLITH TOUCH; URO TOUCH
Manufacturer: NORTHGATE TECHNOLOGIES INC.
Device Classification Name: Lithotriptor, Electro-Hydraulic
Regulation Number: 876.4480
Classification Product Code: FFK
Date Received: 02/14/2013
Decision Date: 11/15/2013
Regulation Medical Specialty: Gastroenterology/Urology

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