meddevicedb.com FDA Device Reference

PROTOCO2L INSUFFLATOR MODEL 6400

K013219 Class II Abbreviated
Decision Date
2002-02-19
Sponsor / Applicant
E-Z-Em, Inc.

Technical Specification

510(k) Submission ID K013219
Product Code FCX
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2002-02-19
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PROTOCO2L INSUFFLATOR MODEL 6400 received FDA 510(k) clearance under submission number K013219, sponsored by E-Z-Em, Inc.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2002-02-19.

Classification & Regulation

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