Vinyl Glove— 510(k) K211904

Name: FDA 510(k) clearance K211904
Creator: U.S. Food and Drug Administration
Published: 2021-09-17

Substantially Equivalent

Jiangsu Dihong Industry and Trade Co., Ltd.

FDA 510(k) clearance K211904 for Vinyl Glove, Substantially Equivalent on 2021-09-17. Applicant: Jiangsu Dihong Industry and Trade Co., Ltd.. Device class: 1.

Clearance details

Applicant: Jiangsu Dihong Industry and Trade Co., Ltd.
Product code: Code LYZ
Device class: Class 1
Regulation: 21 CFR 880.6250
Advisory panel: General Hospital
Date received: 2021-06-21
Decision date: 2021-09-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Shuyang, CN

Download summary PDF View on FDA.gov ↗

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