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FDA 510(k)

SAFETY POWDERFREE BLUE LATEX EXAMINTION GLOVES

K-Number: K980940 · 1998-04-03

Decision Date1998-04-03
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SAFETY POWDERFREE BLUE LATEX EXAMINTION GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Besglove Medicare Sdn. Bhd.. It received FDA 510(k) clearance on 1998-04-03 under 510(k) number K980940. 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 SAFETY POWDERFREE BLUE LATEX EXAMINTION GLOVES?

SAFETY POWDERFREE BLUE LATEX EXAMINTION GLOVES is a medical device that received FDA 510(k) clearance on 1998-04-03. The listed applicant is Besglove Medicare Sdn. Bhd.. The 510(k) number is K980940.

When did SAFETY POWDERFREE BLUE LATEX EXAMINTION GLOVES receive FDA 510(k) clearance?

SAFETY POWDERFREE BLUE LATEX EXAMINTION GLOVES received FDA 510(k) clearance on 1998-04-03, under 510(k) number K980940.

Who is the listed applicant for SAFETY POWDERFREE BLUE LATEX EXAMINTION GLOVES?

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

What is the FDA product code for SAFETY POWDERFREE BLUE LATEX EXAMINTION GLOVES?

The FDA product code for SAFETY POWDERFREE BLUE LATEX EXAMINTION 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 Besglove Medicare 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 22 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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