ENDOSCOPIC RETRIEVAL DEVICE— 510(k) K120084

Name: FDA 510(k) clearance K120084
Creator: U.S. Food and Drug Administration
Published: 2012-05-30

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.. Device class: 2.

Clearance details

Applicant: United States Endoscopy Group, Inc.
Product code: Code OCZ
Device class: Class 2
Regulation: 21 CFR 876.1500
Advisory panel: Gastroenterology, Urology
Date received: 2012-01-11
Decision date: 2012-05-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mentor, OH, US

Download summary PDF View on FDA.gov ↗

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