POWDERED VINYL PATIENT EXAMINATION GLOVES— 510(k) K071686

Name: FDA 510(k) clearance K071686
Creator: U.S. Food and Drug Administration
Published: 2007-08-22

Substantially Equivalent

Langfang Huilong Plastic Product Co., Ltd.

FDA 510(k) clearance K071686 for POWDERED VINYL PATIENT EXAMINATION GLOVES, Substantially Equivalent on 2007-08-22. Applicant: Langfang Huilong Plastic Product Co., Ltd.. Device class: 1.

Clearance details

Applicant: Langfang Huilong Plastic Product Co., Ltd.
Product code: Code LYZ
Device class: Class 1
Regulation: 21 CFR 880.6250
Advisory panel: General Hospital
Date received: 2007-06-20
Decision date: 2007-08-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Haidian Dis, Beijing, CN

Download summary PDF View on FDA.gov ↗

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