meddevicedb.com FDA Device Reference

Uncoated Tubing and Connector Components

K151523 Class II Special
Decision Date
2015-07-16
Sponsor / Applicant
Medtronic, Inc.

Technical Specification

510(k) Submission ID K151523
Product Code DWF
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4210
Decision Date 2015-07-16
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Uncoated Tubing and Connector Components received FDA 510(k) clearance under submission number K151523, sponsored by Medtronic, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2015-07-16.

Classification & Regulation

This clearance is catalogued under FDA product code DWF and 21 CFR 870.4210, within the Cardiovascular review panel as a Class II device.