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FDA 510(k)

CHLORINATED POWDER FREE LATEX EXAMINATION GLOVES (YELLOW)

K-Number: K050277 · 2005-06-07

Decision Date2005-06-07
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CHLORINATED POWDER FREE LATEX EXAMINATION GLOVES (YELLOW) is the device name listed in this FDA 510(k) record. The listed applicant is Hartalega Sdn Bhd. It received FDA 510(k) clearance on 2005-06-07 under 510(k) number K050277. 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 (YELLOW)?

CHLORINATED POWDER FREE LATEX EXAMINATION GLOVES (YELLOW) is a medical device that received FDA 510(k) clearance on 2005-06-07. The listed applicant is Hartalega Sdn Bhd. The 510(k) number is K050277.

When did CHLORINATED POWDER FREE LATEX EXAMINATION GLOVES (YELLOW) receive FDA 510(k) clearance?

CHLORINATED POWDER FREE LATEX EXAMINATION GLOVES (YELLOW) received FDA 510(k) clearance on 2005-06-07, under 510(k) number K050277.

Who is the listed applicant for CHLORINATED POWDER FREE LATEX EXAMINATION GLOVES (YELLOW)?

The FDA 510(k) record lists Hartalega 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 (YELLOW)?

The FDA product code for CHLORINATED POWDER FREE LATEX EXAMINATION GLOVES (YELLOW) 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 Hartalega 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.

View all 55 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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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