meddevicedb.com FDA Device Reference

Reuter Tip Deflecting Wire Guide

K180830 Class II Traditional
Decision Date
2018-12-20
Sponsor / Applicant
Cook Incorporated

Technical Specification

510(k) Submission ID K180830
Product Code DQX
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1330
Decision Date 2018-12-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Reuter Tip Deflecting Wire Guide received FDA 510(k) clearance under submission number K180830, 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 2018-12-20.

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.