AL ASKARI PERCUTANEOUS ACCESS NEEDLE HOLDER— 510(k) K851162

Name: FDA 510(k) clearance K851162
Creator: U.S. Food and Drug Administration
Published: 1985-04-15

Substantially Equivalent

Van-Tec, Inc.

FDA 510(k) clearance K851162 for AL ASKARI PERCUTANEOUS ACCESS NEEDLE HOLDER, Substantially Equivalent on 1985-04-15. Applicant: Van-Tec, Inc.. Device class: 1.

Clearance details

Applicant: Van-Tec, Inc.
Product code: Code KOA
Device class: Class 1
Regulation: 21 CFR 876.4730
Advisory panel: Gastroenterology, Urology
Date received: 1985-03-22
Decision date: 1985-04-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Spencer, IN, US

Download summary PDF View on FDA.gov ↗

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