SHANGHAI GLOVMAX ENTERPRISE CO., LTD. PRE-POWDERED VINYL PATIENT EXAMINATION GLOVES— 510(k) K993859

Name: FDA 510(k) clearance K993859
Creator: U.S. Food and Drug Administration
Published: 2000-01-12

Substantially Equivalent

Shanghai Glovmax Enterprise Co.,Ltd

FDA 510(k) clearance K993859 for SHANGHAI GLOVMAX ENTERPRISE CO., LTD. PRE-POWDERED VINYL PATIENT EXAMINATION GLOVES, Substantially Equivalent on 2000-01-12. Applicant: Shanghai Glovmax Enterprise Co.,Ltd. Device class: 1.

Clearance details

Applicant: Shanghai Glovmax Enterprise Co.,Ltd
Product code: Code LYZ
Device class: Class 1
Regulation: 21 CFR 880.6250
Advisory panel: General Hospital
Date received: 1999-11-15
Decision date: 2000-01-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Taipei, TW

Download summary PDF View on FDA.gov ↗

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