VINYL EXAMINATION GLOVE, POWDER FREE, NON-COLORED
K-Number: K093264 · 2010-05-28
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Device Summary
Frequently Asked Questions
What is the VINYL EXAMINATION GLOVE, POWDER FREE, NON-COLORED?
VINYL EXAMINATION GLOVE, POWDER FREE, NON-COLORED is a medical device that received FDA 510(k) clearance on 2010-05-28. The listed applicant is Qingdao Lang Hui Import & Export Co., Ltd.. The 510(k) number is K093264.
When did VINYL EXAMINATION GLOVE, POWDER FREE, NON-COLORED receive FDA 510(k) clearance?
VINYL EXAMINATION GLOVE, POWDER FREE, NON-COLORED received FDA 510(k) clearance on 2010-05-28, under 510(k) number K093264.
Who is the listed applicant for VINYL EXAMINATION GLOVE, POWDER FREE, NON-COLORED?
The FDA 510(k) record lists Qingdao Lang Hui Import & Export Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VINYL EXAMINATION GLOVE, POWDER FREE, NON-COLORED?
The FDA product code for VINYL EXAMINATION GLOVE, POWDER FREE, NON-COLORED 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 Qingdao Lang Hui Import & Export 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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