meddevicedb.com FDA Device Reference

TorqVue Low Profile Delivery Catheter

K162228 Class II Special
Decision Date
2016-09-09
Sponsor / Applicant
Aga Medical Corporation (Wholly Owned by St.Jude Medical Cor

Technical Specification

510(k) Submission ID K162228
Product Code DQY
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1250
Decision Date 2016-09-09
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TorqVue Low Profile Delivery Catheter received FDA 510(k) clearance under submission number K162228, sponsored by Aga Medical Corporation (Wholly Owned by St.Jude Medical Cor. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2016-09-09.

Classification & Regulation

This clearance is catalogued under FDA product code DQY and 21 CFR 870.1250, within the Cardiovascular review panel as a Class II device.