FUGUAN (BRAND) POWDERED VINYL PATIENT EXAMINATION GLOVES— 510(k) K032907

Name: FDA 510(k) clearance K032907
Creator: U.S. Food and Drug Administration
Published: 2003-11-20

Substantially Equivalent

Shijiazhuang Fuguan Plastic Products Co., Ltd.

FDA 510(k) clearance K032907 for FUGUAN (BRAND) POWDERED VINYL PATIENT EXAMINATION GLOVES, Substantially Equivalent on 2003-11-20. Applicant: Shijiazhuang Fuguan Plastic Products Co., Ltd.. Device class: 1.

Clearance details

Applicant: Shijiazhuang Fuguan Plastic Products Co., Ltd.
Product code: Code LYZ
Device class: Class 1
Regulation: 21 CFR 880.6250
Advisory panel: General Hospital
Date received: 2003-09-17
Decision date: 2003-11-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chaoyang District; Beijing, CN

Download summary PDF View on FDA.gov ↗

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