MODIFIED VAS-CATH CATHETER REPAIR KIT— 510(k) K890099

Name: FDA 510(k) clearance K890099
Creator: U.S. Food and Drug Administration
Published: 1989-04-11

Substantially Equivalent

Vas-Cath, Inc.

FDA 510(k) clearance K890099 for MODIFIED VAS-CATH CATHETER REPAIR KIT, Substantially Equivalent on 1989-04-11. Applicant: Vas-Cath, Inc.. Device class: 2.

Clearance details

Applicant: Vas-Cath, Inc.
Product code: Code LFJ
Device class: Class 2
Regulation: 21 CFR 876.5540
Advisory panel: Gastroenterology, Urology
Date received: 1989-01-10
Decision date: 1989-04-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mississauga, Ontario, 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.