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FDA 510(k)

VINYL EXAMINATION GLOVES, PREPOWDERED USP

K-Number: K984094 · 1999-01-14

ApplicantTrans Ancient Products Co., Ltd.
Decision Date1999-01-14
Product CodeLYZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VINYL EXAMINATION GLOVES, PREPOWDERED USP is the device name listed in this FDA 510(k) record. The listed applicant is Trans Ancient Products Co., Ltd.. It received FDA 510(k) clearance on 1999-01-14 under 510(k) number K984094. The device is classified under product code LYZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VINYL EXAMINATION GLOVES, PREPOWDERED USP?

VINYL EXAMINATION GLOVES, PREPOWDERED USP is a medical device that received FDA 510(k) clearance on 1999-01-14. The listed applicant is Trans Ancient Products Co., Ltd.. The 510(k) number is K984094.

When did VINYL EXAMINATION GLOVES, PREPOWDERED USP receive FDA 510(k) clearance?

VINYL EXAMINATION GLOVES, PREPOWDERED USP received FDA 510(k) clearance on 1999-01-14, under 510(k) number K984094.

Who is the listed applicant for VINYL EXAMINATION GLOVES, PREPOWDERED USP?

The FDA 510(k) record lists Trans Ancient Products Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VINYL EXAMINATION GLOVES, PREPOWDERED USP?

The FDA product code for VINYL EXAMINATION GLOVES, PREPOWDERED USP is LYZ.

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Related Devices (Code: LYZ)

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.

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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.

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