meddevicedb.com FDA Device Reference

CORE E3 Suction/irrigator

K202303 Class II Traditional
Decision Date
2021-02-19
Sponsor / Applicant
Conmed Corporation

Technical Specification

510(k) Submission ID K202303
Product Code GCJ
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2021-02-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CORE E3 Suction/irrigator received FDA 510(k) clearance under submission number K202303, sponsored by Conmed Corporation. 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 2021-02-19.

Classification & Regulation

This clearance is catalogued under FDA product code GCJ and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.