FDA 510(k)

DERMAGRIP POWDER FREE NITRILE EXAMINATION GLOVE, NON STERILE

K-Number: K990752 · 1999-10-18

ApplicantWrp Specialty Products Sdn. Bhd.

Decision Date1999-10-18

Product CodeLZA

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

DERMAGRIP POWDER FREE NITRILE EXAMINATION GLOVE, NON STERILE is the device name listed in this FDA 510(k) record. The listed applicant is Wrp Specialty Products Sdn. Bhd.. It received FDA 510(k) clearance on 1999-10-18 under 510(k) number K990752. 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 DERMAGRIP POWDER FREE NITRILE EXAMINATION GLOVE, NON STERILE?

DERMAGRIP POWDER FREE NITRILE EXAMINATION GLOVE, NON STERILE is a medical device that received FDA 510(k) clearance on 1999-10-18. The listed applicant is Wrp Specialty Products Sdn. Bhd.. The 510(k) number is K990752.

When did DERMAGRIP POWDER FREE NITRILE EXAMINATION GLOVE, NON STERILE receive FDA 510(k) clearance?

DERMAGRIP POWDER FREE NITRILE EXAMINATION GLOVE, NON STERILE received FDA 510(k) clearance on 1999-10-18, under 510(k) number K990752.

Who is the listed applicant for DERMAGRIP POWDER FREE NITRILE EXAMINATION GLOVE, NON STERILE?

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

What is the FDA product code for DERMAGRIP POWDER FREE NITRILE EXAMINATION GLOVE, NON STERILE?

The FDA product code for DERMAGRIP POWDER FREE NITRILE EXAMINATION GLOVE, NON STERILE 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.