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FDA 510(k)

PROFEEL ANATOM SURG GLOVES (POWDER FREE/HYPOALLER)

K-Number: K922515 · 1992-11-25

Decision Date1992-11-25
Product CodeKGO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PROFEEL ANATOM SURG GLOVES (POWDER FREE/HYPOALLER) is the device name listed in this FDA 510(k) record. The listed applicant is Wembley Rubber Products (M) Sdn Bhd. It received FDA 510(k) clearance on 1992-11-25 under 510(k) number K922515. 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 ANATOM SURG GLOVES (POWDER FREE/HYPOALLER)?

PROFEEL ANATOM SURG GLOVES (POWDER FREE/HYPOALLER) is a medical device that received FDA 510(k) clearance on 1992-11-25. The listed applicant is Wembley Rubber Products (M) Sdn Bhd. The 510(k) number is K922515.

When did PROFEEL ANATOM SURG GLOVES (POWDER FREE/HYPOALLER) receive FDA 510(k) clearance?

PROFEEL ANATOM SURG GLOVES (POWDER FREE/HYPOALLER) received FDA 510(k) clearance on 1992-11-25, under 510(k) number K922515.

Who is the listed applicant for PROFEEL ANATOM SURG GLOVES (POWDER FREE/HYPOALLER)?

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

What is the FDA product code for PROFEEL ANATOM SURG GLOVES (POWDER FREE/HYPOALLER)?

The FDA product code for PROFEEL ANATOM SURG GLOVES (POWDER FREE/HYPOALLER) 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 Wembley Rubber Products (M) 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 61 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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