POWDERED VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED)— 510(k) K072084

Name: FDA 510(k) clearance K072084
Creator: U.S. Food and Drug Administration
Published: 2008-05-08

Substantially Equivalent

Zibo Hongye Shangqin Plastic Rubbert Co, Ltd.

FDA 510(k) clearance K072084 for POWDERED VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED), Substantially Equivalent on 2008-05-08. 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: 2008-05-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Beijing, CN

Download summary PDF View on FDA.gov ↗

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K072085 — POWDER FREE VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED)2007-09-04

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