FDA 510(k), K173459, Olympus Small Intestinal Capsule Endoscope System

FDA 510(k), K173459, Olympus Small Intestinal Capsule Endoscope System

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510(K) Number: K173459
Device Name: Olympus Small Intestinal Capsule Endoscope System
Manufacturer: Olympus Medical Systems Corp.
Device Classification Name: system, imaging, gastrointestinal, wireless, capsule
Regulation Number: 876.1300
Classification Product Code: NEZ
Date Received: 11/07/2017
Decision Date: 03/13/2018
Regulation Medical Specialty: Gastroenterology/Urology

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