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FDA 510(k)

POWDER FREE NITRILE EXAMINATION GLOVE

K-Number: K011012 · 2001-05-01

Decision Date2001-05-01
Product CodeLZA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

POWDER FREE NITRILE EXAMINATION GLOVE is the device name listed in this FDA 510(k) record. The listed applicant is Contract Latex Dippers Sdn Bhd. It received FDA 510(k) clearance on 2001-05-01 under 510(k) number K011012. 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 EXAMINATION GLOVE?

POWDER FREE NITRILE EXAMINATION GLOVE is a medical device that received FDA 510(k) clearance on 2001-05-01. The listed applicant is Contract Latex Dippers Sdn Bhd. The 510(k) number is K011012.

When did POWDER FREE NITRILE EXAMINATION GLOVE receive FDA 510(k) clearance?

POWDER FREE NITRILE EXAMINATION GLOVE received FDA 510(k) clearance on 2001-05-01, under 510(k) number K011012.

Who is the listed applicant for POWDER FREE NITRILE EXAMINATION GLOVE?

The FDA 510(k) record lists Contract Latex Dippers Sdn Bhd as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for POWDER FREE NITRILE EXAMINATION GLOVE?

The FDA product code for POWDER FREE NITRILE EXAMINATION GLOVE 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 Contract Latex Dippers 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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