ZOLL AED PRO EXTERNAL DEFIBRILLATOR— 510(k) K041892

Substantially Equivalent

ZOLL Medical Corporation

FDA 510(k) clearance K041892 for ZOLL AED PRO EXTERNAL DEFIBRILLATOR, Substantially Equivalent on 2005-02-04. Applicant: ZOLL Medical Corporation.

Clearance details

Applicant: ZOLL Medical Corporation
Product code: Code MKJ
Advisory panel: Cardiovascular
Date received: 2004-07-13
Decision date: 2005-02-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chelsmford, MA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code MKJ

product code MKJ

Death: 961
Injury: 1,070
Malfunction: 90,719
Other: 8
Total: 92,758

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.