FDA 510(k)

KIMBERLY-CLARK LAVENDER NITRILE POWDER-FREE EXAM GLOVE

K-Number: K131841 · 2013-11-07

Decision Date2013-11-07

Product CodeLZA

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

KIMBERLY-CLARK LAVENDER NITRILE POWDER-FREE EXAM GLOVE is the device name listed in this FDA 510(k) record. The listed applicant is Kimberly-Clark Corp.. It received FDA 510(k) clearance on 2013-11-07 under 510(k) number K131841. The device is classified under product code LZA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KIMBERLY-CLARK LAVENDER NITRILE POWDER-FREE EXAM GLOVE?

KIMBERLY-CLARK LAVENDER NITRILE POWDER-FREE EXAM GLOVE is a medical device that received FDA 510(k) clearance on 2013-11-07. The listed applicant is Kimberly-Clark Corp.. The 510(k) number is K131841.

When did KIMBERLY-CLARK LAVENDER NITRILE POWDER-FREE EXAM GLOVE receive FDA 510(k) clearance?

KIMBERLY-CLARK LAVENDER NITRILE POWDER-FREE EXAM GLOVE received FDA 510(k) clearance on 2013-11-07, under 510(k) number K131841.

Who is the listed applicant for KIMBERLY-CLARK LAVENDER NITRILE POWDER-FREE EXAM GLOVE?

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 LAVENDER NITRILE POWDER-FREE EXAM GLOVE?

The FDA product code for KIMBERLY-CLARK LAVENDER NITRILE POWDER-FREE EXAM GLOVE is LZA.

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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.