BLOOD TUBING SETS (STERILE FLUID PATH)— 510(k) K090255

Name: FDA 510(k) clearance K090255
Creator: U.S. Food and Drug Administration
Published: 2009-02-10

Substantially Equivalent

Nxstage Medical, Inc.

FDA 510(k) clearance K090255 for BLOOD TUBING SETS (STERILE FLUID PATH), Substantially Equivalent on 2009-02-10. Applicant: Nxstage Medical, Inc.. Device class: 2.

Clearance details

Applicant: Nxstage Medical, Inc.
Product code: Code FJK
Device class: Class 2
Regulation: 21 CFR 876.5820
Advisory panel: Gastroenterology, Urology
Date received: 2009-02-02
Decision date: 2009-02-10
Decision: Substantially Equivalent
Clearance type: Special
Location: Lawrence, MA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code FJK

product code FJK

Death: 52
Malfunction: 3,430
Total: 3,482

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.