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FDA 510(k)

MULTISAFE POWDERED LATEX EXAMINATION GLOVES, NONSTERILE

K-Number: K993811 · 2000-03-02

Decision Date2000-03-02
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MULTISAFE POWDERED LATEX EXAMINATION GLOVES, NONSTERILE is the device name listed in this FDA 510(k) record. The listed applicant is Multisafe Sdn. Bhd.. It received FDA 510(k) clearance on 2000-03-02 under 510(k) number K993811. 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 MULTISAFE POWDERED LATEX EXAMINATION GLOVES, NONSTERILE?

MULTISAFE POWDERED LATEX EXAMINATION GLOVES, NONSTERILE is a medical device that received FDA 510(k) clearance on 2000-03-02. The listed applicant is Multisafe Sdn. Bhd.. The 510(k) number is K993811.

When did MULTISAFE POWDERED LATEX EXAMINATION GLOVES, NONSTERILE receive FDA 510(k) clearance?

MULTISAFE POWDERED LATEX EXAMINATION GLOVES, NONSTERILE received FDA 510(k) clearance on 2000-03-02, under 510(k) number K993811.

Who is the listed applicant for MULTISAFE POWDERED LATEX EXAMINATION GLOVES, NONSTERILE?

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

What is the FDA product code for MULTISAFE POWDERED LATEX EXAMINATION GLOVES, NONSTERILE?

The FDA product code for MULTISAFE POWDERED LATEX EXAMINATION GLOVES, NONSTERILE 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 Multisafe 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 8 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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