YULEX LATEX POWDER-FREE EXAM GLOVES— 510(k) K063810

Name: FDA 510(k) clearance K063810
Creator: U.S. Food and Drug Administration
Published: 2008-04-18

Substantially Equivalent

Yulex Corporation

FDA 510(k) clearance K063810 for YULEX LATEX POWDER-FREE EXAM GLOVES, Substantially Equivalent on 2008-04-18. Applicant: Yulex Corporation. Device class: 1.

Clearance details

Applicant: Yulex Corporation
Product code: Code OIG
Device class: Class 1
Regulation: 21 CFR 880.6250
Advisory panel: General Hospital
Date received: 2006-12-22
Decision date: 2008-04-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Maricopa, AZ, US

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