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FDA 510(k) K080403, XTJF TYPE Q160VF1, by Olympus Medical Systems Corporation

FDA 510(k) K080403, XTJF TYPE Q160VF1, by Olympus Medical Systems Corporation

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510(K) Number: K080403
Device Name: XTJF TYPE Q160VF1
Manufacturer: Olympus Medical Systems Corporation
Device Classification Name: duodenoscope and accessories, flexible/rigid
Regulation Number: 876.1500
Classification Product Code: FDT
Date Received: 02/14/2008
Decision Date: 05/20/2008
Regulation Medical Specialty: Gastroenterology/Urology
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