• FDA 510(k) records for MobileRay Pulse SE Digital Imaging System K191503
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FDA 510(k) K130148, FOREIGN BODY HOOD, by United States Endoscopy Group, Inc.

FDA 510(k) K130148, FOREIGN BODY HOOD, by United States Endoscopy Group, Inc.

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510(K) Number: K130148
Device Name: FOREIGN BODY HOOD
Manufacturer: United States Endoscopy Group, Inc.
Device Classification Name: gastroscope and accessories, flexible/rigid
Regulation Number: 876.1500
Classification Product Code: FDS
Date Received: 01/22/2013
Decision Date: 08/07/2013
Regulation Medical Specialty: Gastroenterology/Urology
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