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FDA 510(k)

LEGEND (BRAND) NITRILE POWDER-FREE PATIENT EXAMINATION GLOVE

K-Number: K030529 · 2003-08-08

ApplicantJda (Tianjin) Plastic Rubber Co., Ltd.
Decision Date2003-08-08
Product CodeLZA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LEGEND (BRAND) NITRILE POWDER-FREE PATIENT EXAMINATION GLOVE is the device name listed in this FDA 510(k) record. The listed applicant is Jda (Tianjin) Plastic Rubber Co., Ltd.. It received FDA 510(k) clearance on 2003-08-08 under 510(k) number K030529. 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 LEGEND (BRAND) NITRILE POWDER-FREE PATIENT EXAMINATION GLOVE?

LEGEND (BRAND) NITRILE POWDER-FREE PATIENT EXAMINATION GLOVE is a medical device that received FDA 510(k) clearance on 2003-08-08. The listed applicant is Jda (Tianjin) Plastic Rubber Co., Ltd.. The 510(k) number is K030529.

When did LEGEND (BRAND) NITRILE POWDER-FREE PATIENT EXAMINATION GLOVE receive FDA 510(k) clearance?

LEGEND (BRAND) NITRILE POWDER-FREE PATIENT EXAMINATION GLOVE received FDA 510(k) clearance on 2003-08-08, under 510(k) number K030529.

Who is the listed applicant for LEGEND (BRAND) NITRILE POWDER-FREE PATIENT EXAMINATION GLOVE?

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

What is the FDA product code for LEGEND (BRAND) NITRILE POWDER-FREE PATIENT EXAMINATION GLOVE?

The FDA product code for LEGEND (BRAND) NITRILE POWDER-FREE PATIENT EXAMINATION GLOVE is LZA.

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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.

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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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