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FDA 510(k)

PATIENT VINYL EXAMINATION GLOVES, POWDERFREE, NON-STERILE

K-Number: K083259 · 2009-02-17

ApplicantTangshan Zhongying Plastic Products Co., Ltd.
Decision Date2009-02-17
Product CodeLYZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PATIENT VINYL EXAMINATION GLOVES, POWDERFREE, NON-STERILE is the device name listed in this FDA 510(k) record. The listed applicant is Tangshan Zhongying Plastic Products Co., Ltd.. It received FDA 510(k) clearance on 2009-02-17 under 510(k) number K083259. 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 PATIENT VINYL EXAMINATION GLOVES, POWDERFREE, NON-STERILE?

PATIENT VINYL EXAMINATION GLOVES, POWDERFREE, NON-STERILE is a medical device that received FDA 510(k) clearance on 2009-02-17. The listed applicant is Tangshan Zhongying Plastic Products Co., Ltd.. The 510(k) number is K083259.

When did PATIENT VINYL EXAMINATION GLOVES, POWDERFREE, NON-STERILE receive FDA 510(k) clearance?

PATIENT VINYL EXAMINATION GLOVES, POWDERFREE, NON-STERILE received FDA 510(k) clearance on 2009-02-17, under 510(k) number K083259.

Who is the listed applicant for PATIENT VINYL EXAMINATION GLOVES, POWDERFREE, NON-STERILE?

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

What is the FDA product code for PATIENT VINYL EXAMINATION GLOVES, POWDERFREE, NON-STERILE?

The FDA product code for PATIENT VINYL EXAMINATION GLOVES, POWDERFREE, NON-STERILE 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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