VACCESS 2000 SINGLE LUMEN SUBCLAVIAN CANNULA— 510(k) K844433

Name: FDA 510(k) clearance K844433
Creator: U.S. Food and Drug Administration
Published: 1985-03-13

Substantially Equivalent

Vas-Cath of Canada , Ltd.

FDA 510(k) clearance K844433 for VACCESS 2000 SINGLE LUMEN SUBCLAVIAN CANNULA, Substantially Equivalent on 1985-03-13. Applicant: Vas-Cath of Canada , Ltd.. Device class: 2.

Clearance details

Applicant: Vas-Cath of Canada , Ltd.
Product code: Code LFJ
Device class: Class 2
Regulation: 21 CFR 876.5540
Advisory panel: Gastroenterology, Urology
Date received: 1984-11-16
Decision date: 1985-03-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ontario, L5a 3v3, CA

Download summary PDF View on FDA.gov ↗

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