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FDA 510(k)

STRETCH VINYL EXAMINATION GLOVE, POWDER FREE, YELLOW/WHITE

K-Number: K093263 · 2010-04-30

Decision Date2010-04-30
Product CodeLYZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STRETCH VINYL EXAMINATION GLOVE, POWDER FREE, YELLOW/WHITE is the device name listed in this FDA 510(k) record. The listed applicant is Qingdao Lang Hui Import & Export Co., Ltd.. It received FDA 510(k) clearance on 2010-04-30 under 510(k) number K093263. The device is classified under product code LYZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRETCH VINYL EXAMINATION GLOVE, POWDER FREE, YELLOW/WHITE?

STRETCH VINYL EXAMINATION GLOVE, POWDER FREE, YELLOW/WHITE is a medical device that received FDA 510(k) clearance on 2010-04-30. The listed applicant is Qingdao Lang Hui Import & Export Co., Ltd.. The 510(k) number is K093263.

When did STRETCH VINYL EXAMINATION GLOVE, POWDER FREE, YELLOW/WHITE receive FDA 510(k) clearance?

STRETCH VINYL EXAMINATION GLOVE, POWDER FREE, YELLOW/WHITE received FDA 510(k) clearance on 2010-04-30, under 510(k) number K093263.

Who is the listed applicant for STRETCH VINYL EXAMINATION GLOVE, POWDER FREE, YELLOW/WHITE?

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 STRETCH VINYL EXAMINATION GLOVE, POWDER FREE, YELLOW/WHITE?

The FDA product code for STRETCH VINYL EXAMINATION GLOVE, POWDER FREE, YELLOW/WHITE 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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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