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FDA 510(k)

PATIENT EXAMINATION LATEX GLOVES (NON-STERILE)

K-Number: K911694 · 1991-04-25

Decision Date1991-04-25
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PATIENT EXAMINATION LATEX GLOVES (NON-STERILE) is the device name listed in this FDA 510(k) record. The listed applicant is Guthrie Medicare Products (Melaka) Sdn Bhd. It received FDA 510(k) clearance on 1991-04-25 under 510(k) number K911694. 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 PATIENT EXAMINATION LATEX GLOVES (NON-STERILE)?

PATIENT EXAMINATION LATEX GLOVES (NON-STERILE) is a medical device that received FDA 510(k) clearance on 1991-04-25. The listed applicant is Guthrie Medicare Products (Melaka) Sdn Bhd. The 510(k) number is K911694.

When did PATIENT EXAMINATION LATEX GLOVES (NON-STERILE) receive FDA 510(k) clearance?

PATIENT EXAMINATION LATEX GLOVES (NON-STERILE) received FDA 510(k) clearance on 1991-04-25, under 510(k) number K911694.

Who is the listed applicant for PATIENT EXAMINATION LATEX GLOVES (NON-STERILE)?

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

What is the FDA product code for PATIENT EXAMINATION LATEX GLOVES (NON-STERILE)?

The FDA product code for PATIENT EXAMINATION LATEX GLOVES (NON-STERILE) 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 Guthrie Medicare Products (Melaka) 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 12 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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