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FDA 510(k)

ULTRAFREE TEXTURED STERILE LATEX POWDER-FREE SURGICAL GLOVES

K-Number: K983962 · 1999-01-08

Decision Date1999-01-08
Product CodeKGO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ULTRAFREE TEXTURED STERILE LATEX POWDER-FREE SURGICAL GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Cardinal Health,Medical Products and Services. It received FDA 510(k) clearance on 1999-01-08 under 510(k) number K983962. 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 ULTRAFREE TEXTURED STERILE LATEX POWDER-FREE SURGICAL GLOVES?

ULTRAFREE TEXTURED STERILE LATEX POWDER-FREE SURGICAL GLOVES is a medical device that received FDA 510(k) clearance on 1999-01-08. The listed applicant is Cardinal Health,Medical Products and Services. The 510(k) number is K983962.

When did ULTRAFREE TEXTURED STERILE LATEX POWDER-FREE SURGICAL GLOVES receive FDA 510(k) clearance?

ULTRAFREE TEXTURED STERILE LATEX POWDER-FREE SURGICAL GLOVES received FDA 510(k) clearance on 1999-01-08, under 510(k) number K983962.

Who is the listed applicant for ULTRAFREE TEXTURED STERILE LATEX POWDER-FREE SURGICAL GLOVES?

The FDA 510(k) record lists Cardinal Health,Medical Products and Services as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ULTRAFREE TEXTURED STERILE LATEX POWDER-FREE SURGICAL GLOVES?

The FDA product code for ULTRAFREE TEXTURED STERILE LATEX POWDER-FREE SURGICAL 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.

Other records listing Cardinal Health,Medical Products and Services 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.

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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