meddevicedb.com FDA Device Reference

Heavy Double Flexible Tipped Wire Guide

K150802 Class II Traditional
Decision Date
2015-05-28
Sponsor / Applicant
Cook Incorporated

Technical Specification

510(k) Submission ID K150802
Product Code DQX
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1330
Decision Date 2015-05-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Heavy Double Flexible Tipped Wire Guide received FDA 510(k) clearance under submission number K150802, sponsored by Cook Incorporated. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2015-05-28.

Classification & Regulation

This clearance is catalogued under FDA product code DQX and 21 CFR 870.1330, within the Cardiovascular review panel as a Class II device.