POWDER-FREE VINYL EXAM GLOVES
K-Number: K052006 · 2005-08-03
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Device Summary
Frequently Asked Questions
What is the POWDER-FREE VINYL EXAM GLOVES?
POWDER-FREE VINYL EXAM GLOVES is a medical device that received FDA 510(k) clearance on 2005-08-03. The listed applicant is Baoding Guanzhong Glove Co., Ltd.. The 510(k) number is K052006.
When did POWDER-FREE VINYL EXAM GLOVES receive FDA 510(k) clearance?
POWDER-FREE VINYL EXAM GLOVES received FDA 510(k) clearance on 2005-08-03, under 510(k) number K052006.
Who is the listed applicant for POWDER-FREE VINYL EXAM GLOVES?
The FDA 510(k) record lists Baoding Guanzhong Glove Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for POWDER-FREE VINYL EXAM GLOVES?
The FDA product code for POWDER-FREE VINYL EXAM 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 Baoding Guanzhong Glove 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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