KIMBERLY-CLARK STERLING NITRILE POWDER-FREE EXAM GLOVE (STERILE)
K-Number: K081027 · 2008-06-30
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Device Summary
Frequently Asked Questions
What is the KIMBERLY-CLARK STERLING NITRILE POWDER-FREE EXAM GLOVE (STERILE)?
KIMBERLY-CLARK STERLING NITRILE POWDER-FREE EXAM GLOVE (STERILE) is a medical device that received FDA 510(k) clearance on 2008-06-30. The listed applicant is Kimberly-Clark Corp.. The 510(k) number is K081027.
When did KIMBERLY-CLARK STERLING NITRILE POWDER-FREE EXAM GLOVE (STERILE) receive FDA 510(k) clearance?
KIMBERLY-CLARK STERLING NITRILE POWDER-FREE EXAM GLOVE (STERILE) received FDA 510(k) clearance on 2008-06-30, under 510(k) number K081027.
Who is the listed applicant for KIMBERLY-CLARK STERLING NITRILE POWDER-FREE EXAM GLOVE (STERILE)?
The FDA 510(k) record lists Kimberly-Clark Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KIMBERLY-CLARK STERLING NITRILE POWDER-FREE EXAM GLOVE (STERILE)?
The FDA product code for KIMBERLY-CLARK STERLING NITRILE POWDER-FREE EXAM GLOVE (STERILE) is LZA.
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 Kimberly-Clark Corp. 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: LZA)
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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