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FDA 510(k)

NITRILE EXAMINATION GLOVES, POWDER FREE, GREEN COLOR

K-Number: K990453 · 1999-03-09

Decision Date1999-03-09
Product CodeLZA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NITRILE EXAMINATION GLOVES, POWDER FREE, GREEN COLOR is the device name listed in this FDA 510(k) record. The listed applicant is Alliance Rubber Products Sdn. Bhd.. It received FDA 510(k) clearance on 1999-03-09 under 510(k) number K990453. 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 EXAMINATION GLOVES, POWDER FREE, GREEN COLOR?

NITRILE EXAMINATION GLOVES, POWDER FREE, GREEN COLOR is a medical device that received FDA 510(k) clearance on 1999-03-09. The listed applicant is Alliance Rubber Products Sdn. Bhd.. The 510(k) number is K990453.

When did NITRILE EXAMINATION GLOVES, POWDER FREE, GREEN COLOR receive FDA 510(k) clearance?

NITRILE EXAMINATION GLOVES, POWDER FREE, GREEN COLOR received FDA 510(k) clearance on 1999-03-09, under 510(k) number K990453.

Who is the listed applicant for NITRILE EXAMINATION GLOVES, POWDER FREE, GREEN COLOR?

The FDA 510(k) record lists Alliance Rubber Products Sdn. Bhd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NITRILE EXAMINATION GLOVES, POWDER FREE, GREEN COLOR?

The FDA product code for NITRILE EXAMINATION GLOVES, POWDER FREE, GREEN COLOR 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 Alliance Rubber Products Sdn. Bhd. 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.

View all 12 devices →

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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