PRE-POWDERED VINYL EXAM GLOVE, NON STERILE— 510(k) K994036

Name: FDA 510(k) clearance K994036
Creator: U.S. Food and Drug Administration
Published: 1999-12-20

Substantially Equivalent

Shanghai Champion Plastic Products Co., Ltd.

FDA 510(k) clearance K994036 for PRE-POWDERED VINYL EXAM GLOVE, NON STERILE, Substantially Equivalent on 1999-12-20. Applicant: Shanghai Champion Plastic Products Co., Ltd.. Device class: 1.

Clearance details

Applicant: Shanghai Champion Plastic Products Co., Ltd.
Product code: Code LYZ
Device class: Class 1
Regulation: 21 CFR 880.6250
Advisory panel: General Hospital
Date received: 1999-11-29
Decision date: 1999-12-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sparks, NV, US

Download summary PDF View on FDA.gov ↗

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