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FDA 510(k)

ULTIMAX POWDER FREE EXAMINATION GLOVES

K-Number: K943451 · 1995-02-24

Decision Date1995-02-24
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ULTIMAX POWDER FREE EXAMINATION GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Wembley Rubber Products (M) Sdn Bhd. It received FDA 510(k) clearance on 1995-02-24 under 510(k) number K943451. 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 ULTIMAX POWDER FREE EXAMINATION GLOVES?

ULTIMAX POWDER FREE EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1995-02-24. The listed applicant is Wembley Rubber Products (M) Sdn Bhd. The 510(k) number is K943451.

When did ULTIMAX POWDER FREE EXAMINATION GLOVES receive FDA 510(k) clearance?

ULTIMAX POWDER FREE EXAMINATION GLOVES received FDA 510(k) clearance on 1995-02-24, under 510(k) number K943451.

Who is the listed applicant for ULTIMAX POWDER FREE EXAMINATION GLOVES?

The FDA 510(k) record lists Wembley Rubber Products (M) Sdn Bhd as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ULTIMAX POWDER FREE EXAMINATION GLOVES?

The FDA product code for ULTIMAX POWDER FREE EXAMINATION 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 Wembley Rubber Products (M) 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 61 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

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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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