POWDER-FREE VINYL PATIENT EXAMINATION GLOVES, CLEAR(NON-COLORED)— 510(k) K122893

Name: FDA 510(k) clearance K122893
Creator: U.S. Food and Drug Administration
Published: 2012-11-30

Substantially Equivalent

Geenli Plastic Co, Ltd.

FDA 510(k) clearance K122893 for POWDER-FREE VINYL PATIENT EXAMINATION GLOVES, CLEAR(NON-COLORED), Substantially Equivalent on 2012-11-30. Applicant: Geenli Plastic Co, Ltd.. Device class: 1.

Clearance details

Applicant: Geenli Plastic Co, Ltd.
Product code: Code LYZ
Device class: Class 1
Regulation: 21 CFR 880.6250
Advisory panel: General Hospital
Date received: 2012-09-20
Decision date: 2012-11-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Beijing, CN

Download summary PDF View on FDA.gov ↗

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