KIDNEY TRANSPLANT CATHETER— 510(k) K840687

Name: FDA 510(k) clearance K840687
Creator: U.S. Food and Drug Administration
Published: 1984-06-07

Substantially Equivalent

Warne Surgical Products, Ltd.

FDA 510(k) clearance K840687 for KIDNEY TRANSPLANT CATHETER, Substantially Equivalent on 1984-06-07. Applicant: Warne Surgical Products, Ltd.. Device class: 2.

Clearance details

Applicant: Warne Surgical Products, Ltd.
Product code: Code KDN
Device class: Class 2
Regulation: 21 CFR 876.5880
Advisory panel: Gastroenterology, Urology
Date received: 1984-02-15
Decision date: 1984-06-07
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.