SYNTHETIC, POWDER-FREE VINYL EXAMINATION GLOVES
K-Number: K050450 · 2005-04-04
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Device Summary
Frequently Asked Questions
What is the SYNTHETIC, POWDER-FREE VINYL EXAMINATION GLOVES?
SYNTHETIC, POWDER-FREE VINYL EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 2005-04-04. The listed applicant is Zibo Blue Intco Plastic & Rubber Products Co., Ltd.. The 510(k) number is K050450.
When did SYNTHETIC, POWDER-FREE VINYL EXAMINATION GLOVES receive FDA 510(k) clearance?
SYNTHETIC, POWDER-FREE VINYL EXAMINATION GLOVES received FDA 510(k) clearance on 2005-04-04, under 510(k) number K050450.
Who is the listed applicant for SYNTHETIC, POWDER-FREE VINYL EXAMINATION GLOVES?
The FDA 510(k) record lists Zibo Blue Intco Plastic & Rubber Products Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SYNTHETIC, POWDER-FREE VINYL EXAMINATION GLOVES?
The FDA product code for SYNTHETIC, POWDER-FREE VINYL 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.
Other records listing Zibo Blue Intco Plastic & Rubber Products Co., Ltd. as applicant
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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