meddevicedb.com FDA Device Reference

DSNARE DIMINUTIVE POLYPECTOMY AND SUCTION SYSTEM, MODEL 00711087

K061201 Class II Special
Decision Date
2006-05-30
Sponsor / Applicant
United States Endoscopy Group, Inc.

Technical Specification

510(k) Submission ID K061201
Product Code FCK
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1075
Decision Date 2006-05-30
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DSNARE DIMINUTIVE POLYPECTOMY AND SUCTION SYSTEM, MODEL 00711087 received FDA 510(k) clearance under submission number K061201, sponsored by United States Endoscopy Group, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2006-05-30.

Classification & Regulation

This clearance is catalogued under FDA product code FCK and 21 CFR 876.1075, within the Gastroenterology, Urology review panel as a Class II device.