meddevicedb.com FDA Device Reference

Hi-Torque Command 18 Guide Wire

K152404 Class II Special
Decision Date
2015-09-21
Sponsor / Applicant
Abbott Vascular

Technical Specification

510(k) Submission ID K152404
Product Code DQX
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1330
Decision Date 2015-09-21
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Hi-Torque Command 18 Guide Wire received FDA 510(k) clearance under submission number K152404, sponsored by Abbott Vascular. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2015-09-21.

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.