VINYL POWDERED EXAMINATION GLOVE— 510(k) K091384

Name: FDA 510(k) clearance K091384
Creator: U.S. Food and Drug Administration
Published: 2009-07-20

Substantially Equivalent

Shun Tong Co., Ltd.

FDA 510(k) clearance K091384 for VINYL POWDERED EXAMINATION GLOVE, Substantially Equivalent on 2009-07-20. Applicant: Shun Tong Co., Ltd.. Device class: 1.

Clearance details

Applicant: Shun Tong Co., Ltd.
Product code: Code LYZ
Device class: Class 1
Regulation: 21 CFR 880.6250
Advisory panel: General Hospital
Date received: 2009-05-11
Decision date: 2009-07-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Xinghua City, Jiangsu, CN

Download summary PDF View on FDA.gov ↗

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