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FDA 510(k)

LATEX EXAMINATION GLOVES POWDERED, LOW PROTEIN

K-Number: K991043 · 1999-05-04

Decision Date1999-05-04
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LATEX EXAMINATION GLOVES POWDERED, LOW PROTEIN is the device name listed in this FDA 510(k) record. The listed applicant is Glovco (M) Sdn. Bhd.. It received FDA 510(k) clearance on 1999-05-04 under 510(k) number K991043. 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 LATEX EXAMINATION GLOVES POWDERED, LOW PROTEIN?

LATEX EXAMINATION GLOVES POWDERED, LOW PROTEIN is a medical device that received FDA 510(k) clearance on 1999-05-04. The listed applicant is Glovco (M) Sdn. Bhd.. The 510(k) number is K991043.

When did LATEX EXAMINATION GLOVES POWDERED, LOW PROTEIN receive FDA 510(k) clearance?

LATEX EXAMINATION GLOVES POWDERED, LOW PROTEIN received FDA 510(k) clearance on 1999-05-04, under 510(k) number K991043.

Who is the listed applicant for LATEX EXAMINATION GLOVES POWDERED, LOW PROTEIN?

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

What is the FDA product code for LATEX EXAMINATION GLOVES POWDERED, LOW PROTEIN?

The FDA product code for LATEX EXAMINATION GLOVES POWDERED, LOW PROTEIN 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 Glovco (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 9 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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