POWDERED VINYL EXAMINATION GLOVE— 510(k) K983893

Name: FDA 510(k) clearance K983893
Creator: U.S. Food and Drug Administration
Published: 1999-06-21

Substantially Equivalent

Shijiazhuang Brethern Plastic Co., Ltd.

FDA 510(k) clearance K983893 for POWDERED VINYL EXAMINATION GLOVE, Substantially Equivalent on 1999-06-21. Applicant: Shijiazhuang Brethern Plastic Co., Ltd.. Device class: 1.

Clearance details

Applicant: Shijiazhuang Brethern Plastic Co., Ltd.
Product code: Code LYZ
Device class: Class 1
Regulation: 21 CFR 880.6250
Advisory panel: General Hospital
Date received: 1998-11-02
Decision date: 1999-06-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Shijiazhuang, Hebei, CN

Download summary PDF View on FDA.gov ↗

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