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FDA 510(k)

SAFESKIN NEON NITRILE - POWDER FREE NEON EXAM GLOVE

K-Number: K011713 · 2001-07-05

ApplicantKimberly-Clark Corp.
Decision Date2001-07-05
Product CodeLZA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SAFESKIN NEON NITRILE - POWDER FREE NEON 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 2001-07-05 under 510(k) number K011713. 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 SAFESKIN NEON NITRILE - POWDER FREE NEON EXAM GLOVE?

SAFESKIN NEON NITRILE - POWDER FREE NEON EXAM GLOVE is a medical device that received FDA 510(k) clearance on 2001-07-05. The listed applicant is Kimberly-Clark Corp.. The 510(k) number is K011713.

When did SAFESKIN NEON NITRILE - POWDER FREE NEON EXAM GLOVE receive FDA 510(k) clearance?

SAFESKIN NEON NITRILE - POWDER FREE NEON EXAM GLOVE received FDA 510(k) clearance on 2001-07-05, under 510(k) number K011713.

Who is the listed applicant for SAFESKIN NEON NITRILE - POWDER FREE NEON 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 SAFESKIN NEON NITRILE - POWDER FREE NEON EXAM GLOVE?

The FDA product code for SAFESKIN NEON NITRILE - POWDER FREE NEON EXAM GLOVE is LZA.

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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.

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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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