VINYL EXAMINATION POWDER FREE GLOVES, CLEAR
K-Number: K123590 · 2013-06-17
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Device Summary
Frequently Asked Questions
What is the VINYL EXAMINATION POWDER FREE GLOVES, CLEAR?
VINYL EXAMINATION POWDER FREE GLOVES, CLEAR is a medical device that received FDA 510(k) clearance on 2013-06-17. The listed applicant is Weilin Plastic and Rubber Products Co., Ltd.. The 510(k) number is K123590.
When did VINYL EXAMINATION POWDER FREE GLOVES, CLEAR receive FDA 510(k) clearance?
VINYL EXAMINATION POWDER FREE GLOVES, CLEAR received FDA 510(k) clearance on 2013-06-17, under 510(k) number K123590.
Who is the listed applicant for VINYL EXAMINATION POWDER FREE GLOVES, CLEAR?
The FDA 510(k) record lists Weilin Plastic and Rubber Products Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VINYL EXAMINATION POWDER FREE GLOVES, CLEAR?
The FDA product code for VINYL EXAMINATION POWDER FREE GLOVES, CLEAR is LYZ.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: LYZ)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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