ASAHI NEW PAN-SERIES HEMOFILTERS— 510(k) K844663

Substantially Equivalent

Asahi Medical Co., Ltd.

FDA 510(k) clearance K844663 for ASAHI NEW PAN-SERIES HEMOFILTERS, Substantially Equivalent on 1985-01-18. Applicant: Asahi Medical Co., Ltd..

Clearance details

Applicant: Asahi Medical Co., Ltd.
Product code: Code KDI
Advisory panel: Gastroenterology, Urology
Date received: 1984-11-30
Decision date: 1985-01-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code KDI

product code KDI

Death: 352
Injury: 1,474
Malfunction: 12,534
Other: 4
Total: 14,364

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.