VINYL GLOVE-POWEDERFREE (OBERON GLOVES INTL. LTD)— 510(k) K903847

Name: FDA 510(k) clearance K903847
Creator: U.S. Food and Drug Administration
Published: 1991-01-31

Substantially Equivalent

Zest Mark Industrial Co., Ltd.

FDA 510(k) clearance K903847 for VINYL GLOVE-POWEDERFREE (OBERON GLOVES INTL. LTD), Substantially Equivalent on 1991-01-31. Applicant: Zest Mark Industrial Co., Ltd.. Device class: 1.

Clearance details

Applicant: Zest Mark Industrial Co., Ltd.
Product code: Code LYZ
Device class: Class 1
Regulation: 21 CFR 880.6250
Advisory panel: General Hospital
Date received: 1990-08-21
Decision date: 1991-01-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Taiwan, Roc, TW

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.