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FDA 510(k)

GUTHRIE PRIME PRE-POWDERED PATIENT LATEX EXAMINATION GLOVE

K-Number: K993793 · 2000-01-12

Decision Date2000-01-12
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

GUTHRIE PRIME PRE-POWDERED PATIENT LATEX EXAMINATION GLOVE 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 2000-01-12 under 510(k) number K993793. 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 GUTHRIE PRIME PRE-POWDERED PATIENT LATEX EXAMINATION GLOVE?

GUTHRIE PRIME PRE-POWDERED PATIENT LATEX EXAMINATION GLOVE is a medical device that received FDA 510(k) clearance on 2000-01-12. The listed applicant is Guthrie Medicare Products (Melaka) Sdn Bhd. The 510(k) number is K993793.

When did GUTHRIE PRIME PRE-POWDERED PATIENT LATEX EXAMINATION GLOVE receive FDA 510(k) clearance?

GUTHRIE PRIME PRE-POWDERED PATIENT LATEX EXAMINATION GLOVE received FDA 510(k) clearance on 2000-01-12, under 510(k) number K993793.

Who is the listed applicant for GUTHRIE PRIME PRE-POWDERED PATIENT LATEX EXAMINATION GLOVE?

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 GUTHRIE PRIME PRE-POWDERED PATIENT LATEX EXAMINATION GLOVE?

The FDA product code for GUTHRIE PRIME PRE-POWDERED PATIENT 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.

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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