VINYL PATIENT EXAMINATION GLOVES-PRE-POWDERED— 510(k) K982257

Name: FDA 510(k) clearance K982257
Creator: U.S. Food and Drug Administration
Published: 1998-08-03

Substantially Equivalent

Taian Plastics Products (Jingxing) Co., Ltd.

FDA 510(k) clearance K982257 for VINYL PATIENT EXAMINATION GLOVES-PRE-POWDERED, Substantially Equivalent on 1998-08-03. Applicant: Taian Plastics Products (Jingxing) Co., Ltd.. Device class: 1.

Clearance details

Applicant: Taian Plastics Products (Jingxing) Co., Ltd.
Product code: Code LYZ
Device class: Class 1
Regulation: 21 CFR 880.6250
Advisory panel: General Hospital
Date received: 1998-06-26
Decision date: 1998-08-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Shijiazhuang City, Hebei Prov., CN

Download summary PDF View on FDA.gov ↗

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