EIKEN KIZAI ARTIFICIAL KIDNEY BLOOD CIR— 510(k) K823733

Substantially Equivalent

Advocacy International, Ltd.

FDA 510(k) clearance K823733 for EIKEN KIZAI ARTIFICIAL KIDNEY BLOOD CIR, Substantially Equivalent on 1983-01-14. Applicant: Advocacy International, Ltd..

Clearance details

Applicant: Advocacy International, Ltd.
Product code: Code KOC
Advisory panel: Gastroenterology, Urology
Date received: 1982-12-13
Decision date: 1983-01-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code KOC

product code KOC

Death: 4
Total: 4

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.