meddevicedb.com FDA Device Reference

APPROACH CTO WIRE GUIDE

K081337 Class II Special
Decision Date
2008-08-08
Sponsor / Applicant
Cook Incorporated

Technical Specification

510(k) Submission ID K081337
Product Code DQX
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1330
Decision Date 2008-08-08
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

APPROACH CTO WIRE GUIDE received FDA 510(k) clearance under submission number K081337, sponsored by Cook Incorporated. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2008-08-08.

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.