POWDER FREE VINYL PATIENT EXAMINATION GLOVES— 510(k) K942042

Name: FDA 510(k) clearance K942042
Creator: U.S. Food and Drug Administration
Published: 1994-08-05

Substantially Equivalent

Cheer & Merit Co., Ltd.

FDA 510(k) clearance K942042 for POWDER FREE VINYL PATIENT EXAMINATION GLOVES, Substantially Equivalent on 1994-08-05. Applicant: Cheer & Merit Co., Ltd.. Device class: 1.

Clearance details

Applicant: Cheer & Merit Co., Ltd.
Product code: Code LYZ
Device class: Class 1
Regulation: 21 CFR 880.6250
Advisory panel: General Hospital
Date received: 1994-04-28
Decision date: 1994-08-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Great Neck, NY, US

Download summary PDF View on FDA.gov ↗

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