FDA 510(k)

NUGARD NITRIL POWDERFREE NITRILE EXAMINATION GLOVE

K-Number: K990840 · 1999-05-17

Decision Date1999-05-17

Product CodeLZA

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

NUGARD NITRIL POWDERFREE NITRILE EXAMINATION GLOVE is the device name listed in this FDA 510(k) record. The listed applicant is Terang Nusa Sdn Bhd. It received FDA 510(k) clearance on 1999-05-17 under 510(k) number K990840. 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 NUGARD NITRIL POWDERFREE NITRILE EXAMINATION GLOVE?

NUGARD NITRIL POWDERFREE NITRILE EXAMINATION GLOVE is a medical device that received FDA 510(k) clearance on 1999-05-17. The listed applicant is Terang Nusa Sdn Bhd. The 510(k) number is K990840.

When did NUGARD NITRIL POWDERFREE NITRILE EXAMINATION GLOVE receive FDA 510(k) clearance?

NUGARD NITRIL POWDERFREE NITRILE EXAMINATION GLOVE received FDA 510(k) clearance on 1999-05-17, under 510(k) number K990840.

Who is the listed applicant for NUGARD NITRIL POWDERFREE NITRILE EXAMINATION GLOVE?

The FDA 510(k) record lists Terang Nusa Sdn Bhd as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NUGARD NITRIL POWDERFREE NITRILE EXAMINATION GLOVE?

The FDA product code for NUGARD NITRIL POWDERFREE NITRILE EXAMINATION GLOVE is LZA.

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Related Devices (Code: 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.