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FDA 510(k)

NITRILE PATIENT EXAMINATION GLOVES, POWDER-FREE AND YELLOWISH WHITE

K-Number: K014284 · 2002-02-15

Decision Date2002-02-15
Product CodeLZA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NITRILE PATIENT EXAMINATION GLOVES, POWDER-FREE AND YELLOWISH WHITE is the device name listed in this FDA 510(k) record. The listed applicant is Formosa Glove Industrial Co., Ltd.. It received FDA 510(k) clearance on 2002-02-15 under 510(k) number K014284. 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 NITRILE PATIENT EXAMINATION GLOVES, POWDER-FREE AND YELLOWISH WHITE?

NITRILE PATIENT EXAMINATION GLOVES, POWDER-FREE AND YELLOWISH WHITE is a medical device that received FDA 510(k) clearance on 2002-02-15. The listed applicant is Formosa Glove Industrial Co., Ltd.. The 510(k) number is K014284.

When did NITRILE PATIENT EXAMINATION GLOVES, POWDER-FREE AND YELLOWISH WHITE receive FDA 510(k) clearance?

NITRILE PATIENT EXAMINATION GLOVES, POWDER-FREE AND YELLOWISH WHITE received FDA 510(k) clearance on 2002-02-15, under 510(k) number K014284.

Who is the listed applicant for NITRILE PATIENT EXAMINATION GLOVES, POWDER-FREE AND YELLOWISH WHITE?

The FDA 510(k) record lists Formosa Glove Industrial Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NITRILE PATIENT EXAMINATION GLOVES, POWDER-FREE AND YELLOWISH WHITE?

The FDA product code for NITRILE PATIENT EXAMINATION GLOVES, POWDER-FREE AND YELLOWISH WHITE 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 Formosa Glove Industrial Co., Ltd. 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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