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FDA 510(k)

SKIN GUARD, POWDER FREE LATEX EXAMINATION GLOVES, NON-STERILE

K-Number: K111923 · 2011-11-04

Decision Date2011-11-04
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SKIN GUARD, POWDER FREE LATEX EXAMINATION GLOVES, NON-STERILE is the device name listed in this FDA 510(k) record. The listed applicant is Pt. Intan Hevea Industry. It received FDA 510(k) clearance on 2011-11-04 under 510(k) number K111923. 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 SKIN GUARD, POWDER FREE LATEX EXAMINATION GLOVES, NON-STERILE?

SKIN GUARD, POWDER FREE LATEX EXAMINATION GLOVES, NON-STERILE is a medical device that received FDA 510(k) clearance on 2011-11-04. The listed applicant is Pt. Intan Hevea Industry. The 510(k) number is K111923.

When did SKIN GUARD, POWDER FREE LATEX EXAMINATION GLOVES, NON-STERILE receive FDA 510(k) clearance?

SKIN GUARD, POWDER FREE LATEX EXAMINATION GLOVES, NON-STERILE received FDA 510(k) clearance on 2011-11-04, under 510(k) number K111923.

Who is the listed applicant for SKIN GUARD, POWDER FREE LATEX EXAMINATION GLOVES, NON-STERILE?

The FDA 510(k) record lists Pt. Intan Hevea Industry as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SKIN GUARD, POWDER FREE LATEX EXAMINATION GLOVES, NON-STERILE?

The FDA product code for SKIN GUARD, POWDER FREE LATEX EXAMINATION GLOVES, NON-STERILE 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 Pt. Intan Hevea Industry 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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