meddevicedb.com FDA Device Reference

Single Use Electrosurgical Snare SD-400

K172734 Class II Traditional
Decision Date
2017-12-07
Sponsor / Applicant
Olympus Medical Systems Corp.

Technical Specification

510(k) Submission ID K172734
Product Code FDI
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.4300
Decision Date 2017-12-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Single Use Electrosurgical Snare SD-400 received FDA 510(k) clearance under submission number K172734, sponsored by Olympus Medical Systems Corp.. 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 2017-12-07.

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.