• FDA 510(k) records for MobileRay Pulse SE Digital Imaging System K191503
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FDA 510(k) K120084, ENDOSCOPIC RETRIEVAL DEVICE, by United States Endoscopy Group, Inc.

FDA 510(k) K120084, ENDOSCOPIC RETRIEVAL DEVICE, by United States Endoscopy Group, Inc.

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510(K) Number: K120084
Device Name: ENDOSCOPIC RETRIEVAL DEVICE
Manufacturer: United States Endoscopy Group, Inc.
Device Classification Name: endoscopic grasping/cutting instrument, non-powered
Regulation Number: 876.1500
Classification Product Code: OCZ
Date Received: 01/11/2012
Decision Date: 05/30/2012
Regulation Medical Specialty: Gastroenterology/Urology
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