ENDOSCOPIC RETRIEVAL DEVICE— 510(k) K120084

Substantially Equivalent

United States Endoscopy Group, Inc.

FDA 510(k) clearance K120084 for ENDOSCOPIC RETRIEVAL DEVICE, Substantially Equivalent on 2012-05-30. Applicant: United States Endoscopy Group, Inc..

Clearance details

Applicant: United States Endoscopy Group, Inc.
Product code: Code OCZ
Advisory panel: Gastroenterology, Urology
Date received: 2012-01-11
Decision date: 2012-05-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mentor, OH, US

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