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FDA 510(k)

LATEX EXAMINATION GLOVES, POWDER FREE

K-Number: K930602 · 1993-09-29

Decision Date1993-09-29
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LATEX EXAMINATION GLOVES, POWDER FREE is the device name listed in this FDA 510(k) record. The listed applicant is Tekmedic (M) Sdn Bhd. It received FDA 510(k) clearance on 1993-09-29 under 510(k) number K930602. The device is classified under product code LYY. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LATEX EXAMINATION GLOVES, POWDER FREE?

LATEX EXAMINATION GLOVES, POWDER FREE is a medical device that received FDA 510(k) clearance on 1993-09-29. The listed applicant is Tekmedic (M) Sdn Bhd. The 510(k) number is K930602.

When did LATEX EXAMINATION GLOVES, POWDER FREE receive FDA 510(k) clearance?

LATEX EXAMINATION GLOVES, POWDER FREE received FDA 510(k) clearance on 1993-09-29, under 510(k) number K930602.

Who is the listed applicant for LATEX EXAMINATION GLOVES, POWDER FREE?

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

What is the FDA product code for LATEX EXAMINATION GLOVES, POWDER FREE?

The FDA product code for LATEX EXAMINATION GLOVES, POWDER FREE is LYY.

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 Tekmedic (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 11 devices →

Related Devices (Code: LYY)

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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