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FDA 510(k)

DUNFORD SURGEON'S STERILE GLOVES

K-Number: K880480 · 1988-06-17

Decision Date1988-06-17
Product CodeKGO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DUNFORD SURGEON'S STERILE GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Phillippine Radiant C/O U.S. Polymer Industries. It received FDA 510(k) clearance on 1988-06-17 under 510(k) number K880480. 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 DUNFORD SURGEON'S STERILE GLOVES?

DUNFORD SURGEON'S STERILE GLOVES is a medical device that received FDA 510(k) clearance on 1988-06-17. The listed applicant is Phillippine Radiant C/O U.S. Polymer Industries. The 510(k) number is K880480.

When did DUNFORD SURGEON'S STERILE GLOVES receive FDA 510(k) clearance?

DUNFORD SURGEON'S STERILE GLOVES received FDA 510(k) clearance on 1988-06-17, under 510(k) number K880480.

Who is the listed applicant for DUNFORD SURGEON'S STERILE GLOVES?

The FDA 510(k) record lists Phillippine Radiant C/O U.S. Polymer Industries as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DUNFORD SURGEON'S STERILE GLOVES?

The FDA product code for DUNFORD SURGEON'S STERILE 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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