2006, 2010, 2011, 2012(CARDIAC DC DEFIBRILLATOR)— 510(k) K852799

Name: FDA 510(k) clearance K852799
Creator: U.S. Food and Drug Administration
Published: 1985-09-16

Substantially Equivalent

Cardiac Recorders, Ltd.

FDA 510(k) clearance K852799 for 2006, 2010, 2011, 2012(CARDIAC DC DEFIBRILLATOR), Substantially Equivalent on 1985-09-16. Applicant: Cardiac Recorders, Ltd.. Device class: 2.

Clearance details

Applicant: Cardiac Recorders, Ltd.
Product code: Code LDD
Device class: Class 2
Regulation: 21 CFR 870.5300
Advisory panel: Cardiovascular
Date received: 1985-07-01
Decision date: 1985-09-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: London, GB

Download summary PDF View on FDA.gov ↗

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Adverse events under product code LDD

product code LDD

Death: 38
Malfunction: 522
Total: 560

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.