SHOCK ADVISORY ADAPTER FOR USE W/LIFEPAK 9— 510(k) K892005

Substantially Equivalent

Physio-Control Corp.

FDA 510(k) clearance K892005 for SHOCK ADVISORY ADAPTER FOR USE W/LIFEPAK 9, Substantially Equivalent on 1989-06-20. Applicant: Physio-Control Corp..

Clearance details

Applicant: Physio-Control Corp.
Product code: Code MKJ
Advisory panel: Cardiovascular
Date received: 1989-03-28
Decision date: 1989-06-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Redmond, 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.