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FDA 510(k)

POWDERED, NATURAL COLOR, LATEX EXAMINATION GLOVE MODEL: MEP1

K-Number: K101106 · 2010-11-10

Decision Date2010-11-10
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

POWDERED, NATURAL COLOR, LATEX EXAMINATION GLOVE MODEL: MEP1 is the device name listed in this FDA 510(k) record. The listed applicant is Best Putra Gloves Sdn Bhd. It received FDA 510(k) clearance on 2010-11-10 under 510(k) number K101106. 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 POWDERED, NATURAL COLOR, LATEX EXAMINATION GLOVE MODEL: MEP1?

POWDERED, NATURAL COLOR, LATEX EXAMINATION GLOVE MODEL: MEP1 is a medical device that received FDA 510(k) clearance on 2010-11-10. The listed applicant is Best Putra Gloves Sdn Bhd. The 510(k) number is K101106.

When did POWDERED, NATURAL COLOR, LATEX EXAMINATION GLOVE MODEL: MEP1 receive FDA 510(k) clearance?

POWDERED, NATURAL COLOR, LATEX EXAMINATION GLOVE MODEL: MEP1 received FDA 510(k) clearance on 2010-11-10, under 510(k) number K101106.

Who is the listed applicant for POWDERED, NATURAL COLOR, LATEX EXAMINATION GLOVE MODEL: MEP1?

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

What is the FDA product code for POWDERED, NATURAL COLOR, LATEX EXAMINATION GLOVE MODEL: MEP1?

The FDA product code for POWDERED, NATURAL COLOR, LATEX EXAMINATION GLOVE MODEL: MEP1 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 Best Putra 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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