Clearance Summary
ST. JUDE MEDICAL, CPS DUO LEFT HEART LEAD DELIVERY SYSTEM received FDA 510(k) clearance under submission number K072864, sponsored by St. Jude Medical, Cardiac Rhythm Management Divisi. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2008-03-13.
- Submission: K072864
- Applicant / Sponsor: St. Jude Medical, Cardiac Rhythm Management Divisi
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1380
- Decision date: 2008-03-13
Classification & Regulation
This clearance is catalogued under FDA product code DRB and 21 CFR 870.1380, within the Cardiovascular review panel as a Class II device.