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FDA 510(k)

POWDER FREE LATEX EXAM GLOVES

K-Number: K925685 · 1993-06-25

Decision Date1993-06-25
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

POWDER FREE LATEX EXAM GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is M.M. Rubber Co. , Ltd.. It received FDA 510(k) clearance on 1993-06-25 under 510(k) number K925685. 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 EXAM GLOVES?

POWDER FREE LATEX EXAM GLOVES is a medical device that received FDA 510(k) clearance on 1993-06-25. The listed applicant is M.M. Rubber Co. , Ltd.. The 510(k) number is K925685.

When did POWDER FREE LATEX EXAM GLOVES receive FDA 510(k) clearance?

POWDER FREE LATEX EXAM GLOVES received FDA 510(k) clearance on 1993-06-25, under 510(k) number K925685.

Who is the listed applicant for POWDER FREE LATEX EXAM GLOVES?

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

What is the FDA product code for POWDER FREE LATEX EXAM GLOVES?

The FDA product code for POWDER FREE LATEX EXAM GLOVES 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 M.M. Rubber Co. , Ltd. 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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