POWDER FREE VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED)— 510(k) K072085

Name: FDA 510(k) clearance K072085
Creator: U.S. Food and Drug Administration
Published: 2007-09-04

Substantially Equivalent

Zibo Hongye Shangqin Plastic Rubbert Co, Ltd.

FDA 510(k) clearance K072085 for POWDER FREE VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED), Substantially Equivalent on 2007-09-04. Applicant: Zibo Hongye Shangqin Plastic Rubbert Co, Ltd.. Device class: 1.

Clearance details

Applicant: Zibo Hongye Shangqin Plastic Rubbert Co, Ltd.
Product code: Code LYZ
Device class: Class 1
Regulation: 21 CFR 880.6250
Advisory panel: General Hospital
Date received: 2007-07-30
Decision date: 2007-09-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Beijing, CN

Download summary PDF View on FDA.gov ↗

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K072084 — POWDERED VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED)2008-05-08

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