VAS-CATH PEDIATRIC HEMOFILTRATION CATHETER— 510(k) K882466

Name: FDA 510(k) clearance K882466
Creator: U.S. Food and Drug Administration
Published: 1988-07-13

Substantially Equivalent

Vas-Cath, Inc.

FDA 510(k) clearance K882466 for VAS-CATH PEDIATRIC HEMOFILTRATION CATHETER, Substantially Equivalent on 1988-07-13. Applicant: Vas-Cath, Inc.. Device class: 2.

Clearance details

Applicant: Vas-Cath, Inc.
Product code: Code LFK
Device class: Class 2
Regulation: 21 CFR 876.5540
Advisory panel: Gastroenterology, Urology
Date received: 1988-06-15
Decision date: 1988-07-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mississauga, Ontario, CA

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