POWDER-FREE VINYL PATIENT EXAMINATION GLOVES
K-Number: K092790 · 2009-11-02
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Device Summary
Frequently Asked Questions
What is the POWDER-FREE VINYL PATIENT EXAMINATION GLOVES?
POWDER-FREE VINYL PATIENT EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 2009-11-02. The listed applicant is Zibo Boxiang Plastic & Rubber Co., Ltd.. The 510(k) number is K092790.
When did POWDER-FREE VINYL PATIENT EXAMINATION GLOVES receive FDA 510(k) clearance?
POWDER-FREE VINYL PATIENT EXAMINATION GLOVES received FDA 510(k) clearance on 2009-11-02, under 510(k) number K092790.
Who is the listed applicant for POWDER-FREE VINYL PATIENT EXAMINATION GLOVES?
The FDA 510(k) record lists Zibo Boxiang Plastic & Rubber Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for POWDER-FREE VINYL PATIENT EXAMINATION GLOVES?
The FDA product code for POWDER-FREE VINYL PATIENT EXAMINATION GLOVES 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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