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FDA 510(k)

POWDER NITRILE EXAMINATION GLOVE (WHITE AND BLUE COLOR)

K-Number: K063522 · 2007-02-08

Decision Date2007-02-08
Product CodeLZA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

POWDER NITRILE EXAMINATION GLOVE (WHITE AND BLUE COLOR) is the device name listed in this FDA 510(k) record. The listed applicant is Hl Rubber Industries Sdn Bhd. It received FDA 510(k) clearance on 2007-02-08 under 510(k) number K063522. 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 NITRILE EXAMINATION GLOVE (WHITE AND BLUE COLOR)?

POWDER NITRILE EXAMINATION GLOVE (WHITE AND BLUE COLOR) is a medical device that received FDA 510(k) clearance on 2007-02-08. The listed applicant is Hl Rubber Industries Sdn Bhd. The 510(k) number is K063522.

When did POWDER NITRILE EXAMINATION GLOVE (WHITE AND BLUE COLOR) receive FDA 510(k) clearance?

POWDER NITRILE EXAMINATION GLOVE (WHITE AND BLUE COLOR) received FDA 510(k) clearance on 2007-02-08, under 510(k) number K063522.

Who is the listed applicant for POWDER NITRILE EXAMINATION GLOVE (WHITE AND BLUE COLOR)?

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

What is the FDA product code for POWDER NITRILE EXAMINATION GLOVE (WHITE AND BLUE COLOR)?

The FDA product code for POWDER NITRILE EXAMINATION GLOVE (WHITE AND BLUE 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 Hl Rubber Industries 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.

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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