PVC EXAMINATION GLOVES— 510(k) K894752

Name: FDA 510(k) clearance K894752
Creator: U.S. Food and Drug Administration
Published: 1990-01-11

Substantially Equivalent

Dan Dong Linsen Plastic Industrial Co., Ltd.

FDA 510(k) clearance K894752 for PVC EXAMINATION GLOVES, Substantially Equivalent on 1990-01-11. Applicant: Dan Dong Linsen Plastic Industrial Co., Ltd.. Device class: 1.

Clearance details

Applicant: Dan Dong Linsen Plastic Industrial Co., Ltd.
Product code: Code LYZ
Device class: Class 1
Regulation: 21 CFR 880.6250
Advisory panel: General Hospital
Date received: 1989-07-26
Decision date: 1990-01-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Liaoning Province, China, CN

Download summary PDF View on FDA.gov ↗

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