HEMOFILTRATION CATHETER HF-100— 510(k) K840322

Name: FDA 510(k) clearance K840322
Creator: U.S. Food and Drug Administration
Published: 1984-04-24

Substantially Equivalent

Vas-Cath of Canada , Ltd.

FDA 510(k) clearance K840322 for HEMOFILTRATION CATHETER HF-100, Substantially Equivalent on 1984-04-24. Applicant: Vas-Cath of Canada , Ltd.. Device class: 2.

Clearance details

Applicant: Vas-Cath of Canada , Ltd.
Product code: Code FIQ
Device class: Class 2
Regulation: 21 CFR 876.5540
Advisory panel: Gastroenterology, Urology
Date received: 1984-01-25
Decision date: 1984-04-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.