POWDERED VINYL PATIENT EXAMINATION GLOVES WHITE (NON-COLORED)— 510(k) K051923

Name: FDA 510(k) clearance K051923
Creator: U.S. Food and Drug Administration
Published: 2005-08-16

Substantially Equivalent

Shijiazhuang Wonder Plastic Co., Ltd.

FDA 510(k) clearance K051923 for POWDERED VINYL PATIENT EXAMINATION GLOVES WHITE (NON-COLORED), Substantially Equivalent on 2005-08-16. Applicant: Shijiazhuang Wonder Plastic Co., Ltd.. Device class: 1.

Clearance details

Applicant: Shijiazhuang Wonder Plastic Co., Ltd.
Product code: Code LYZ
Device class: Class 1
Regulation: 21 CFR 880.6250
Advisory panel: General Hospital
Date received: 2005-07-15
Decision date: 2005-08-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Haidian Dis, Beijing, CN

Download summary PDF View on FDA.gov ↗

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