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FDA 510(k)

CHLORINATED POWDER-FREE LATEX EXAMINATION GLOVES, (BLUE, GREEN)

K-Number: K010854 · 2001-06-13

Decision Date2001-06-13
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CHLORINATED POWDER-FREE LATEX EXAMINATION GLOVES, (BLUE, GREEN) is the device name listed in this FDA 510(k) record. The listed applicant is Protection Gloves Sdn. Bhd.. It received FDA 510(k) clearance on 2001-06-13 under 510(k) number K010854. The device is classified under product code LYY. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHLORINATED POWDER-FREE LATEX EXAMINATION GLOVES, (BLUE, GREEN)?

CHLORINATED POWDER-FREE LATEX EXAMINATION GLOVES, (BLUE, GREEN) is a medical device that received FDA 510(k) clearance on 2001-06-13. The listed applicant is Protection Gloves Sdn. Bhd.. The 510(k) number is K010854.

When did CHLORINATED POWDER-FREE LATEX EXAMINATION GLOVES, (BLUE, GREEN) receive FDA 510(k) clearance?

CHLORINATED POWDER-FREE LATEX EXAMINATION GLOVES, (BLUE, GREEN) received FDA 510(k) clearance on 2001-06-13, under 510(k) number K010854.

Who is the listed applicant for CHLORINATED POWDER-FREE LATEX EXAMINATION GLOVES, (BLUE, GREEN)?

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

What is the FDA product code for CHLORINATED POWDER-FREE LATEX EXAMINATION GLOVES, (BLUE, GREEN)?

The FDA product code for CHLORINATED POWDER-FREE LATEX EXAMINATION GLOVES, (BLUE, GREEN) is LYY.

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 Protection Gloves 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: LYY)

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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