Disposable Vinyl Examination Glove— 510(k) K220469

Name: FDA 510(k) clearance K220469
Creator: U.S. Food and Drug Administration
Published: 2022-06-16

Substantially Equivalent

Chifeng Huawei Medical Science&Technology Co., Ltd.

FDA 510(k) clearance K220469 for Disposable Vinyl Examination Glove, Substantially Equivalent on 2022-06-16. Applicant: Chifeng Huawei Medical Science&Technology Co., Ltd.. Device class: 1.

Clearance details

Applicant: Chifeng Huawei Medical Science&Technology Co., Ltd.
Product code: Code LYZ
Device class: Class 1
Regulation: 21 CFR 880.6250
Advisory panel: General Hospital
Date received: 2022-02-18
Decision date: 2022-06-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chifeng, CN

Download summary PDF View on FDA.gov ↗

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