SUNMAX ENTERPRISE SHANGHAI VINYL POWDERED PATIENT EXAM. GLOVES— 510(k) K960746

Name: FDA 510(k) clearance K960746
Creator: U.S. Food and Drug Administration
Published: 1996-06-27

Substantially Equivalent

Sunmax Enterprise Shanghai Co. , Ltd.

FDA 510(k) clearance K960746 for SUNMAX ENTERPRISE SHANGHAI VINYL POWDERED PATIENT EXAM. GLOVES, Substantially Equivalent on 1996-06-27. Applicant: Sunmax Enterprise Shanghai Co. , Ltd.. Device class: 1.

Clearance details

Applicant: Sunmax Enterprise Shanghai Co. , Ltd.
Product code: Code LYZ
Device class: Class 1
Regulation: 21 CFR 880.6250
Advisory panel: General Hospital
Date received: 1996-02-23
Decision date: 1996-06-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Great Neck,, NY, US

Download summary PDF View on FDA.gov ↗

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