meddevicedb.com FDA Device Reference

SJM CONFIRM

K122161 Class II Traditional
Decision Date
2012-11-28
Sponsor / Applicant
St Jude Medical

Technical Specification

510(k) Submission ID K122161
Product Code MXC
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2800
Decision Date 2012-11-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SJM CONFIRM received FDA 510(k) clearance under submission number K122161, sponsored by St Jude Medical. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2012-11-28.

Classification & Regulation

This clearance is catalogued under FDA product code MXC and 21 CFR 870.2800, within the Cardiovascular review panel as a Class II device.