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FDA 510(k)

POWDERED LATEX SURGEON'S GLOVES

K-Number: K031368 · 2004-06-22

Decision Date2004-06-22
Product CodeKGO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

POWDERED LATEX SURGEON'S GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Cephas Medical Private , Ltd.. It received FDA 510(k) clearance on 2004-06-22 under 510(k) number K031368. The device is classified under product code KGO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POWDERED LATEX SURGEON'S GLOVES?

POWDERED LATEX SURGEON'S GLOVES is a medical device that received FDA 510(k) clearance on 2004-06-22. The listed applicant is Cephas Medical Private , Ltd.. The 510(k) number is K031368.

When did POWDERED LATEX SURGEON'S GLOVES receive FDA 510(k) clearance?

POWDERED LATEX SURGEON'S GLOVES received FDA 510(k) clearance on 2004-06-22, under 510(k) number K031368.

Who is the listed applicant for POWDERED LATEX SURGEON'S GLOVES?

The FDA 510(k) record lists Cephas Medical Private , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for POWDERED LATEX SURGEON'S GLOVES?

The FDA product code for POWDERED LATEX SURGEON'S GLOVES is KGO.

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.

Related Devices (Code: KGO)

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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