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UROLOGY MONOPOLAR SNARE FOR TISSUE TRANSECTION

K103611 Class II Traditional
Decision Date
2011-05-09
Sponsor / Applicant
United States Endoscopy Group, Inc.

Technical Specification

510(k) Submission ID K103611
Product Code FDI
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.4300
Decision Date 2011-05-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

UROLOGY MONOPOLAR SNARE FOR TISSUE TRANSECTION received FDA 510(k) clearance under submission number K103611, sponsored by United States Endoscopy Group, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2011-05-09.

Classification & Regulation

This clearance is catalogued under FDA product code FDI and 21 CFR 876.4300, within the Gastroenterology, Urology review panel as a Class II device.