DOUBLE LUMEN SUBCLAVIN CATHETER SC-400— 510(k) K810745

Name: FDA 510(k) clearance K810745
Creator: U.S. Food and Drug Administration
Published: 1981-03-31

Substantially Equivalent

Vas-Cath of Canada , Ltd.

FDA 510(k) clearance K810745 for DOUBLE LUMEN SUBCLAVIN CATHETER SC-400, Substantially Equivalent on 1981-03-31. 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: 1981-03-19
Decision date: 1981-03-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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