meddevicedb.com FDA Device Reference

TRACER METRO SMART WIRE GUIDE

K033754 Class II Special
Decision Date
2003-12-30
Sponsor / Applicant
Wilson-Cook Medical, Inc.

Technical Specification

510(k) Submission ID K033754
Product Code OCY
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2003-12-30
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TRACER METRO SMART WIRE GUIDE received FDA 510(k) clearance under submission number K033754, sponsored by Wilson-Cook Medical, 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 2003-12-30.

Classification & Regulation

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