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FDA 510(k)

PROTEXIS LATEX BASIC STERILE POWDER-FREE SURGICAL GLOVES

K-Number: K121897 · 2012-07-27

Decision Date2012-07-27
Product CodeKGO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PROTEXIS LATEX BASIC STERILE POWDER-FREE SURGICAL GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Cardinal Health, Inc.. It received FDA 510(k) clearance on 2012-07-27 under 510(k) number K121897. 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 PROTEXIS LATEX BASIC STERILE POWDER-FREE SURGICAL GLOVES?

PROTEXIS LATEX BASIC STERILE POWDER-FREE SURGICAL GLOVES is a medical device that received FDA 510(k) clearance on 2012-07-27. The listed applicant is Cardinal Health, Inc.. The 510(k) number is K121897.

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

PROTEXIS LATEX BASIC STERILE POWDER-FREE SURGICAL GLOVES received FDA 510(k) clearance on 2012-07-27, under 510(k) number K121897.

Who is the listed applicant for PROTEXIS LATEX BASIC STERILE POWDER-FREE SURGICAL GLOVES?

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

What is the FDA product code for PROTEXIS LATEX BASIC STERILE POWDER-FREE SURGICAL GLOVES?

The FDA product code for PROTEXIS LATEX BASIC STERILE 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, Inc. 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 26 devices →

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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