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FDA 510(k)

POWDERED SYNTHETIC VINYL PATIENT EXAMINATION GLOVES, WHITE

K-Number: K030200 · 2003-03-20

Decision Date2003-03-20
Product CodeLYZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

POWDERED SYNTHETIC VINYL PATIENT EXAMINATION GLOVES, WHITE is the device name listed in this FDA 510(k) record. The listed applicant is Kaohsiung Brothers Products Corp.. It received FDA 510(k) clearance on 2003-03-20 under 510(k) number K030200. 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 POWDERED SYNTHETIC VINYL PATIENT EXAMINATION GLOVES, WHITE?

POWDERED SYNTHETIC VINYL PATIENT EXAMINATION GLOVES, WHITE is a medical device that received FDA 510(k) clearance on 2003-03-20. The listed applicant is Kaohsiung Brothers Products Corp.. The 510(k) number is K030200.

When did POWDERED SYNTHETIC VINYL PATIENT EXAMINATION GLOVES, WHITE receive FDA 510(k) clearance?

POWDERED SYNTHETIC VINYL PATIENT EXAMINATION GLOVES, WHITE received FDA 510(k) clearance on 2003-03-20, under 510(k) number K030200.

Who is the listed applicant for POWDERED SYNTHETIC VINYL PATIENT EXAMINATION GLOVES, WHITE?

The FDA 510(k) record lists Kaohsiung Brothers Products Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for POWDERED SYNTHETIC VINYL PATIENT EXAMINATION GLOVES, WHITE?

The FDA product code for POWDERED SYNTHETIC VINYL PATIENT EXAMINATION GLOVES, WHITE is LYZ.

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 Kaohsiung Brothers Products Corp. 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.

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.

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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