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FDA 510(k)

POWDER-FREE LATEX EXAMINATION GLOVES WITH COLORANTS

K-Number: K020818 · 2002-07-05

Decision Date2002-07-05
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

POWDER-FREE LATEX EXAMINATION GLOVES WITH COLORANTS is the device name listed in this FDA 510(k) record. The listed applicant is Allegiance Healthcare Corp.. It received FDA 510(k) clearance on 2002-07-05 under 510(k) number K020818. 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 POWDER-FREE LATEX EXAMINATION GLOVES WITH COLORANTS?

POWDER-FREE LATEX EXAMINATION GLOVES WITH COLORANTS is a medical device that received FDA 510(k) clearance on 2002-07-05. The listed applicant is Allegiance Healthcare Corp.. The 510(k) number is K020818.

When did POWDER-FREE LATEX EXAMINATION GLOVES WITH COLORANTS receive FDA 510(k) clearance?

POWDER-FREE LATEX EXAMINATION GLOVES WITH COLORANTS received FDA 510(k) clearance on 2002-07-05, under 510(k) number K020818.

Who is the listed applicant for POWDER-FREE LATEX EXAMINATION GLOVES WITH COLORANTS?

The FDA 510(k) record lists Allegiance Healthcare Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for POWDER-FREE LATEX EXAMINATION GLOVES WITH COLORANTS?

The FDA product code for POWDER-FREE LATEX EXAMINATION GLOVES WITH COLORANTS 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 Allegiance Healthcare Corp. 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 63 devices →

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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