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FDA 510(k)

POWDERED LATEX EXAMINATION GLOVES

K-Number: K013026 · 2001-10-15

Decision Date2001-10-15
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

POWDERED LATEX EXAMINATION GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Great Glove (Thailand) Co. , Ltd.. It received FDA 510(k) clearance on 2001-10-15 under 510(k) number K013026. The device is classified under product code LYY. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POWDERED LATEX EXAMINATION GLOVES?

POWDERED LATEX EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 2001-10-15. The listed applicant is Great Glove (Thailand) Co. , Ltd.. The 510(k) number is K013026.

When did POWDERED LATEX EXAMINATION GLOVES receive FDA 510(k) clearance?

POWDERED LATEX EXAMINATION GLOVES received FDA 510(k) clearance on 2001-10-15, under 510(k) number K013026.

Who is the listed applicant for POWDERED LATEX EXAMINATION GLOVES?

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

What is the FDA product code for POWDERED LATEX EXAMINATION GLOVES?

The FDA product code for POWDERED LATEX EXAMINATION GLOVES is LYY.

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 (Thailand) 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: LYY)

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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