meddevicedb.com FDA Device Reference

ULTIMUM/ENGAGE/ENGAGE TR

K091137 Class II Traditional
Decision Date
2009-04-22
Sponsor / Applicant
St Jude Medical

Technical Specification

510(k) Submission ID K091137
Product Code DYB
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1340
Decision Date 2009-04-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ULTIMUM/ENGAGE/ENGAGE TR received FDA 510(k) clearance under submission number K091137, 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 2009-04-22.

Classification & Regulation

This clearance is catalogued under FDA product code DYB and 21 CFR 870.1340, within the Cardiovascular review panel as a Class II device.