meddevicedb.com FDA Device Reference

IRRIGATION/ASPIRATION POLYPECTOMY

K970356 Class II Traditional
Decision Date
1997-03-25
Sponsor / Applicant
United States Endoscopy Group, Inc.

Technical Specification

510(k) Submission ID K970356
Product Code FDI
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.4300
Decision Date 1997-03-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IRRIGATION/ASPIRATION POLYPECTOMY received FDA 510(k) clearance under submission number K970356, 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 1997-03-25.

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.