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FDA 510(k)

POWDERED LATEX EXAMINATION GLOVES

K-Number: K033531 · 2004-03-03

Decision Date2004-03-03
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 Apl International Incorporated Limited. It received FDA 510(k) clearance on 2004-03-03 under 510(k) number K033531. 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 2004-03-03. The listed applicant is Apl International Incorporated Limited. The 510(k) number is K033531.

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

POWDERED LATEX EXAMINATION GLOVES received FDA 510(k) clearance on 2004-03-03, under 510(k) number K033531.

Who is the listed applicant for POWDERED LATEX EXAMINATION GLOVES?

The FDA 510(k) record lists Apl International Incorporated Limited 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 Apl International Incorporated Limited 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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