SYNTHETIC POWDER FREE VINYL PATIENT EXAM GLOVES— 510(k) K022639

Name: FDA 510(k) clearance K022639
Creator: U.S. Food and Drug Administration
Published: 2002-09-16

Substantially Equivalent

Shijiazhuang Holy Plastics Co., Ltd.

FDA 510(k) clearance K022639 for SYNTHETIC POWDER FREE VINYL PATIENT EXAM GLOVES, Substantially Equivalent on 2002-09-16. Applicant: Shijiazhuang Holy Plastics Co., Ltd.. Device class: 1.

Clearance details

Applicant: Shijiazhuang Holy Plastics Co., Ltd.
Product code: Code LYZ
Device class: Class 1
Regulation: 21 CFR 880.6250
Advisory panel: General Hospital
Date received: 2002-08-08
Decision date: 2002-09-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mc Henry, IL, US

Download summary PDF View on FDA.gov ↗

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