PRE-POWDERED VINYL EXAM GLOVES— 510(k) K041379

Name: FDA 510(k) clearance K041379
Creator: U.S. Food and Drug Administration
Published: 2004-08-31

Substantially Equivalent

Shijiazhuang Wally Plastics Co., Ltd.

FDA 510(k) clearance K041379 for PRE-POWDERED VINYL EXAM GLOVES, Substantially Equivalent on 2004-08-31. Applicant: Shijiazhuang Wally Plastics Co., Ltd.. Device class: 1.

Clearance details

Applicant: Shijiazhuang Wally Plastics Co., Ltd.
Product code: Code LYZ
Device class: Class 1
Regulation: 21 CFR 880.6250
Advisory panel: General Hospital
Date received: 2004-05-24
Decision date: 2004-08-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Jinzhou City, Hebei, CN

Download summary PDF View on FDA.gov ↗

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