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FDA 510(k)

POWDER-FREE NITRILE EXAM GLOVE, LAVENDER/PURPLE

K-Number: K003563 · 2001-01-02

Decision Date2001-01-02
Product CodeLZA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

POWDER-FREE NITRILE EXAM GLOVE, LAVENDER/PURPLE is the device name listed in this FDA 510(k) record. The listed applicant is Ning BO Yujiang Rubber & Plastic Co.. It received FDA 510(k) clearance on 2001-01-02 under 510(k) number K003563. The device is classified under product code LZA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POWDER-FREE NITRILE EXAM GLOVE, LAVENDER/PURPLE?

POWDER-FREE NITRILE EXAM GLOVE, LAVENDER/PURPLE is a medical device that received FDA 510(k) clearance on 2001-01-02. The listed applicant is Ning BO Yujiang Rubber & Plastic Co.. The 510(k) number is K003563.

When did POWDER-FREE NITRILE EXAM GLOVE, LAVENDER/PURPLE receive FDA 510(k) clearance?

POWDER-FREE NITRILE EXAM GLOVE, LAVENDER/PURPLE received FDA 510(k) clearance on 2001-01-02, under 510(k) number K003563.

Who is the listed applicant for POWDER-FREE NITRILE EXAM GLOVE, LAVENDER/PURPLE?

The FDA 510(k) record lists Ning BO Yujiang Rubber & Plastic Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for POWDER-FREE NITRILE EXAM GLOVE, LAVENDER/PURPLE?

The FDA product code for POWDER-FREE NITRILE EXAM GLOVE, LAVENDER/PURPLE is LZA.

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 Ning BO Yujiang Rubber & Plastic Co. 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: LZA)

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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