DISPOSABLE POWDERED VINYL EXAM GLOVES— 510(k) K032190

Name: FDA 510(k) clearance K032190
Creator: U.S. Food and Drug Administration
Published: 2003-08-14

Substantially Equivalent

Synmertex Co, Ltd.

FDA 510(k) clearance K032190 for DISPOSABLE POWDERED VINYL EXAM GLOVES, Substantially Equivalent on 2003-08-14. Applicant: Synmertex Co, Ltd.. Device class: 1.

Clearance details

Applicant: Synmertex Co, Ltd.
Product code: Code LYZ
Device class: Class 1
Regulation: 21 CFR 880.6250
Advisory panel: General Hospital
Date received: 2003-07-17
Decision date: 2003-08-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rowland Heights, CA, US

Download summary PDF View on FDA.gov ↗

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