meddevicedb.com FDA Device Reference

CPS DIRECT SL II SLITTABLE OUTER CATHETER

K103250 Class II Special
Decision Date
2011-01-19
Sponsor / Applicant
St. Jude Medical, Cardiac Rhythm Management Divisi

Technical Specification

510(k) Submission ID K103250
Product Code DQY
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1250
Decision Date 2011-01-19
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CPS DIRECT SL II SLITTABLE OUTER CATHETER received FDA 510(k) clearance under submission number K103250, sponsored by St. Jude Medical, Cardiac Rhythm Management Divisi. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2011-01-19.

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.