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FDA 510(k)

DISPOSABLE PVC EXAMINATION GLOVE, POWDERED AND POWDER-FREE

K-Number: K053259 · 2006-01-18

ApplicantPractical Protective Plastic Manufactory , Ltd.
Decision Date2006-01-18
Product CodeLYZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE PVC EXAMINATION GLOVE, POWDERED AND POWDER-FREE is the device name listed in this FDA 510(k) record. The listed applicant is Practical Protective Plastic Manufactory , Ltd.. It received FDA 510(k) clearance on 2006-01-18 under 510(k) number K053259. 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 DISPOSABLE PVC EXAMINATION GLOVE, POWDERED AND POWDER-FREE?

DISPOSABLE PVC EXAMINATION GLOVE, POWDERED AND POWDER-FREE is a medical device that received FDA 510(k) clearance on 2006-01-18. The listed applicant is Practical Protective Plastic Manufactory , Ltd.. The 510(k) number is K053259.

When did DISPOSABLE PVC EXAMINATION GLOVE, POWDERED AND POWDER-FREE receive FDA 510(k) clearance?

DISPOSABLE PVC EXAMINATION GLOVE, POWDERED AND POWDER-FREE received FDA 510(k) clearance on 2006-01-18, under 510(k) number K053259.

Who is the listed applicant for DISPOSABLE PVC EXAMINATION GLOVE, POWDERED AND POWDER-FREE?

The FDA 510(k) record lists Practical Protective Plastic Manufactory , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DISPOSABLE PVC EXAMINATION GLOVE, POWDERED AND POWDER-FREE?

The FDA product code for DISPOSABLE PVC EXAMINATION GLOVE, POWDERED AND POWDER-FREE is LYZ.

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Related Devices (Code: LYZ)

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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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