HEARTSTREAM FR2 AED, MODEL M3860A,M3861A— 510(k) K003565

Substantially Equivalent

Agilent Technologies, Inc.

FDA 510(k) clearance K003565 for HEARTSTREAM FR2 AED, MODEL M3860A,M3861A, Substantially Equivalent on 2000-12-20. Applicant: Agilent Technologies, Inc..

Clearance details

Applicant: Agilent Technologies, Inc.
Product code: Code MKJ
Advisory panel: Cardiovascular
Date received: 2000-11-20
Decision date: 2000-12-20
Decision: Substantially Equivalent
Clearance type: Special
Location: Seattle, WA, US

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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.