FDA 510(k), K091773, FUJINON STERILE OVERTUBES

FDA 510(k), K091773, FUJINON STERILE OVERTUBES

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510(K) Number: K091773
Device Name: FUJINON STERILE OVERTUBES
Manufacturer: FUJINON, INC.
Device Classification Name: endoscopic access overtube, gastroenterology-urology
Regulation Number: 876.1500
Classification Product Code: FED
Date Received: 06/16/2009
Decision Date: 08/07/2009
Regulation Medical Specialty: Gastroenterology/Urology

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