VINYL PATIENT EXAMINATION GLOVE, POWDERED— 510(k) K971423

Name: FDA 510(k) clearance K971423
Creator: U.S. Food and Drug Administration
Published: 1997-05-23

Substantially Equivalent

Shanghai Foremost Plastic Industrial Co., Ltd.

FDA 510(k) clearance K971423 for VINYL PATIENT EXAMINATION GLOVE, POWDERED, Substantially Equivalent on 1997-05-23. Applicant: Shanghai Foremost Plastic Industrial Co., Ltd.. Device class: 1.

Clearance details

Applicant: Shanghai Foremost Plastic Industrial Co., Ltd.
Product code: Code LYZ
Device class: Class 1
Regulation: 21 CFR 880.6250
Advisory panel: General Hospital
Date received: 1997-04-17
Decision date: 1997-05-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Songjiang County, Shanghai, CN

Download summary PDF View on FDA.gov ↗

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