PROTEGRITY SMT LATEX SURGICALGLOVES
K-Number: K101811 · 2010-10-15
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Device Summary
Frequently Asked Questions
What is the PROTEGRITY SMT LATEX SURGICALGLOVES?
PROTEGRITY SMT LATEX SURGICALGLOVES is a medical device that received FDA 510(k) clearance on 2010-10-15. The listed applicant is Cardinal Health, Inc.. The 510(k) number is K101811.
When did PROTEGRITY SMT LATEX SURGICALGLOVES receive FDA 510(k) clearance?
PROTEGRITY SMT LATEX SURGICALGLOVES received FDA 510(k) clearance on 2010-10-15, under 510(k) number K101811.
Who is the listed applicant for PROTEGRITY SMT LATEX SURGICALGLOVES?
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 PROTEGRITY SMT LATEX SURGICALGLOVES?
The FDA product code for PROTEGRITY SMT LATEX SURGICALGLOVES 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.
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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