2000 SERIES PORTABLE RESUSCITATION SYST.— 510(k) K812519

Substantially Equivalent

Life Science Instrumentation, Inc.

FDA 510(k) clearance K812519 for 2000 SERIES PORTABLE RESUSCITATION SYST., Substantially Equivalent on 1981-09-25. Applicant: Life Science Instrumentation, Inc..

Clearance details

Applicant: Life Science Instrumentation, Inc.
Product code: Code LDD
Advisory panel: Cardiovascular
Date received: 1981-09-02
Decision date: 1981-09-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

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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.