POWDER FREE VINYL EXAMINATION GLOVE— 510(k) K032071

Name: FDA 510(k) clearance K032071
Creator: U.S. Food and Drug Administration
Published: 2003-10-10

Substantially Equivalent

Shanghai Foremost Plastic Industrial Co., Ltd.

FDA 510(k) clearance K032071 for POWDER FREE VINYL EXAMINATION GLOVE, Substantially Equivalent on 2003-10-10. Applicant: Shanghai Foremost Plastic Industrial Co., Ltd.. Device class: 1.

Clearance details

Applicant: Shanghai Foremost Plastic Industrial Co., Ltd.
Product code: Code LYZ
Device class: Class 1
Regulation: 21 CFR 880.6250
Advisory panel: General Hospital
Date received: 2003-07-03
Decision date: 2003-10-10
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Palm Harbor, FL, US

Download summary PDF View on FDA.gov ↗

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