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FDA 510(k)

VINYL EXAMINATION GLOVES, POWDERED

K-Number: K033308 · 2003-12-22

ApplicantTangshan Transocean Plastic Products Co., Ltd.
Decision Date2003-12-22
Product CodeLYZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VINYL EXAMINATION GLOVES, POWDERED is the device name listed in this FDA 510(k) record. The listed applicant is Tangshan Transocean Plastic Products Co., Ltd.. It received FDA 510(k) clearance on 2003-12-22 under 510(k) number K033308. 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 VINYL EXAMINATION GLOVES, POWDERED?

VINYL EXAMINATION GLOVES, POWDERED is a medical device that received FDA 510(k) clearance on 2003-12-22. The listed applicant is Tangshan Transocean Plastic Products Co., Ltd.. The 510(k) number is K033308.

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

VINYL EXAMINATION GLOVES, POWDERED received FDA 510(k) clearance on 2003-12-22, under 510(k) number K033308.

Who is the listed applicant for VINYL EXAMINATION GLOVES, POWDERED?

The FDA 510(k) record lists Tangshan Transocean Plastic Products Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VINYL EXAMINATION GLOVES, POWDERED?

The FDA product code for VINYL EXAMINATION GLOVES, POWDERED is LYZ.

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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.

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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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