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FDA 510(k)

MEDLINE NITRILE EXAM GLOVES W/ALOE -GREEN

K-Number: K090568 · 2009-10-02

ApplicantMedline Industries, Inc.
Decision Date2009-10-02
Product CodeLZA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MEDLINE NITRILE EXAM GLOVES W/ALOE -GREEN is the device name listed in this FDA 510(k) record. The listed applicant is Medline Industries, Inc.. It received FDA 510(k) clearance on 2009-10-02 under 510(k) number K090568. 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 MEDLINE NITRILE EXAM GLOVES W/ALOE -GREEN?

MEDLINE NITRILE EXAM GLOVES W/ALOE -GREEN is a medical device that received FDA 510(k) clearance on 2009-10-02. The listed applicant is Medline Industries, Inc.. The 510(k) number is K090568.

When did MEDLINE NITRILE EXAM GLOVES W/ALOE -GREEN receive FDA 510(k) clearance?

MEDLINE NITRILE EXAM GLOVES W/ALOE -GREEN received FDA 510(k) clearance on 2009-10-02, under 510(k) number K090568.

Who is the listed applicant for MEDLINE NITRILE EXAM GLOVES W/ALOE -GREEN?

The FDA 510(k) record lists Medline Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDLINE NITRILE EXAM GLOVES W/ALOE -GREEN?

The FDA product code for MEDLINE NITRILE EXAM GLOVES W/ALOE -GREEN is LZA.

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Related Devices (Code: LZA)

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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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