STERILE NEOPRENE POWDER-FREE SURGICAL GLOVES WITH NITRILE COATING
K-Number: K102500 · 2010-11-04
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Device Summary
Frequently Asked Questions
What is the STERILE NEOPRENE POWDER-FREE SURGICAL GLOVES WITH NITRILE COATING?
STERILE NEOPRENE POWDER-FREE SURGICAL GLOVES WITH NITRILE COATING is a medical device that received FDA 510(k) clearance on 2010-11-04. The listed applicant is Cardinal Health, Inc.. The 510(k) number is K102500.
When did STERILE NEOPRENE POWDER-FREE SURGICAL GLOVES WITH NITRILE COATING receive FDA 510(k) clearance?
STERILE NEOPRENE POWDER-FREE SURGICAL GLOVES WITH NITRILE COATING received FDA 510(k) clearance on 2010-11-04, under 510(k) number K102500.
Who is the listed applicant for STERILE NEOPRENE POWDER-FREE SURGICAL GLOVES WITH NITRILE COATING?
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 STERILE NEOPRENE POWDER-FREE SURGICAL GLOVES WITH NITRILE COATING?
The FDA product code for STERILE NEOPRENE POWDER-FREE SURGICAL GLOVES WITH NITRILE COATING 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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