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FDA 510(k)

PROFEEL POWDER FREE NITRILE SURGICAL GLOVE, STERILE

K-Number: K000971 · 2000-04-14

Decision Date2000-04-14
Product CodeKGO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PROFEEL POWDER FREE NITRILE SURGICAL GLOVE, STERILE is the device name listed in this FDA 510(k) record. The listed applicant is Wrp Asia Pacific Sdn. Bhd.. It received FDA 510(k) clearance on 2000-04-14 under 510(k) number K000971. The device is classified under product code KGO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROFEEL POWDER FREE NITRILE SURGICAL GLOVE, STERILE?

PROFEEL POWDER FREE NITRILE SURGICAL GLOVE, STERILE is a medical device that received FDA 510(k) clearance on 2000-04-14. The listed applicant is Wrp Asia Pacific Sdn. Bhd.. The 510(k) number is K000971.

When did PROFEEL POWDER FREE NITRILE SURGICAL GLOVE, STERILE receive FDA 510(k) clearance?

PROFEEL POWDER FREE NITRILE SURGICAL GLOVE, STERILE received FDA 510(k) clearance on 2000-04-14, under 510(k) number K000971.

Who is the listed applicant for PROFEEL POWDER FREE NITRILE SURGICAL GLOVE, STERILE?

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

What is the FDA product code for PROFEEL POWDER FREE NITRILE SURGICAL GLOVE, STERILE?

The FDA product code for PROFEEL POWDER FREE NITRILE SURGICAL GLOVE, STERILE is KGO.

Related Clinical Trials

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.

Other records listing Wrp Asia Pacific Sdn. Bhd. as applicant

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.

View all 44 devices →

Related Devices (Code: KGO)

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.

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.

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