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FDA 510(k)

POWDER-FREE LATEX EXAMINATION GLOVE

K-Number: K952473 · 1995-10-12

Decision Date1995-10-12
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

POWDER-FREE LATEX EXAMINATION GLOVE is the device name listed in this FDA 510(k) record. The listed applicant is M.M.R. Gloves Private , Ltd.. It received FDA 510(k) clearance on 1995-10-12 under 510(k) number K952473. 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 GLOVE?

POWDER-FREE LATEX EXAMINATION GLOVE is a medical device that received FDA 510(k) clearance on 1995-10-12. The listed applicant is M.M.R. Gloves Private , Ltd.. The 510(k) number is K952473.

When did POWDER-FREE LATEX EXAMINATION GLOVE receive FDA 510(k) clearance?

POWDER-FREE LATEX EXAMINATION GLOVE received FDA 510(k) clearance on 1995-10-12, under 510(k) number K952473.

Who is the listed applicant for POWDER-FREE LATEX EXAMINATION GLOVE?

The FDA 510(k) record lists M.M.R. Gloves Private , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for POWDER-FREE LATEX EXAMINATION GLOVE?

The FDA product code for POWDER-FREE LATEX EXAMINATION GLOVE 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.

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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