NIPRO PUREFLUX-L HEMODIALYZER— 510(k) K122952

Name: FDA 510(k) clearance K122952
Creator: U.S. Food and Drug Administration
Published: 2013-12-04

Substantially Equivalent

Nipro Medical Corporation

FDA 510(k) clearance K122952 for NIPRO PUREFLUX-L HEMODIALYZER, Substantially Equivalent on 2013-12-04. Applicant: Nipro Medical Corporation. Device class: 2.

Clearance details

Applicant: Nipro Medical Corporation
Product code: Code FJI
Device class: Class 2
Regulation: 21 CFR 876.5820
Advisory panel: Gastroenterology, Urology
Date received: 2012-09-25
Decision date: 2013-12-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Suwanee, GA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code FJI

product code FJI

Death: 2
Total: 2

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.