SJM CONFIRM IMPLANTABLE CARDIAC MONITOR— 510(k) K122090

Name: FDA 510(k) clearance K122090
Creator: U.S. Food and Drug Administration
Published: 2012-11-15

Substantially Equivalent

St. Jude Medical, Cardiac Rhythm Management Divisi

FDA 510(k) clearance K122090 for SJM CONFIRM IMPLANTABLE CARDIAC MONITOR, Substantially Equivalent on 2012-11-15. Applicant: St. Jude Medical, Cardiac Rhythm Management Divisi. Device class: 2.

Clearance details

Applicant: St. Jude Medical, Cardiac Rhythm Management Divisi
Product code: Code MXC
Device class: Class 2
Regulation: 21 CFR 870.2800
Advisory panel: Cardiovascular
Date received: 2012-07-16
Decision date: 2012-11-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sylmar, CA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code MXC

product code MXC

Death: 4
Injury: 758
Malfunction: 5,066
Total: 5,828

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.