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FDA 510(k)

GREAT GLOVE POWDER FREE VINYL EXAMINATION GLOVES

K-Number: K052923 · 2005-12-21

Decision Date2005-12-21
Product CodeLYZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

GREAT GLOVE POWDER FREE VINYL EXAMINATION GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Great Glove (China), Inc.. It received FDA 510(k) clearance on 2005-12-21 under 510(k) number K052923. 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 GREAT GLOVE POWDER FREE VINYL EXAMINATION GLOVES?

GREAT GLOVE POWDER FREE VINYL EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 2005-12-21. The listed applicant is Great Glove (China), Inc.. The 510(k) number is K052923.

When did GREAT GLOVE POWDER FREE VINYL EXAMINATION GLOVES receive FDA 510(k) clearance?

GREAT GLOVE POWDER FREE VINYL EXAMINATION GLOVES received FDA 510(k) clearance on 2005-12-21, under 510(k) number K052923.

Who is the listed applicant for GREAT GLOVE POWDER FREE VINYL EXAMINATION GLOVES?

The FDA 510(k) record lists Great Glove (China), Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GREAT GLOVE POWDER FREE VINYL EXAMINATION GLOVES?

The FDA product code for GREAT GLOVE 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 Great Glove (China), Inc. 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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