HIGH FLUX HEMODIALYSIS MEMBRANE DIALYZER OR HIGH FLUX HOLLOW FIBER DIALYZER, MODELS APS-R, -M, -S, -E, AND -EX— 510(k) K041726

Substantially Equivalent

Asahi Medical Co., Ltd.

FDA 510(k) clearance K041726 for HIGH FLUX HEMODIALYSIS MEMBRANE DIALYZER OR HIGH FLUX HOLLOW FIBER DIALYZER, MODELS APS-R, -M, -S, -E, AND -EX, Substantially Equivalent on 2004-07-23. Applicant: Asahi Medical Co., Ltd..

Clearance details

Applicant: Asahi Medical Co., Ltd.
Product code: Code KDI
Advisory panel: Gastroenterology, Urology
Date received: 2004-06-25
Decision date: 2004-07-23
Decision: Substantially Equivalent
Clearance type: Special
Location: Rockville, MD, US

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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.