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FDA 510(k)

BROTHERS POWDERED SYNTHETIC VINYL PATIENT EXAMINATION GLOVES, YELLOW

K-Number: K032323 · 2003-10-07

Decision Date2003-10-07
Product CodeLYZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BROTHERS POWDERED SYNTHETIC VINYL PATIENT EXAMINATION GLOVES, YELLOW is the device name listed in this FDA 510(k) record. The listed applicant is Long First (Xiamen) Plastics Co., Ltd.. It received FDA 510(k) clearance on 2003-10-07 under 510(k) number K032323. 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 BROTHERS POWDERED SYNTHETIC VINYL PATIENT EXAMINATION GLOVES, YELLOW?

BROTHERS POWDERED SYNTHETIC VINYL PATIENT EXAMINATION GLOVES, YELLOW is a medical device that received FDA 510(k) clearance on 2003-10-07. The listed applicant is Long First (Xiamen) Plastics Co., Ltd.. The 510(k) number is K032323.

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

BROTHERS POWDERED SYNTHETIC VINYL PATIENT EXAMINATION GLOVES, YELLOW received FDA 510(k) clearance on 2003-10-07, under 510(k) number K032323.

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

The FDA 510(k) record lists Long First (Xiamen) Plastics Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

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

The FDA product code for BROTHERS POWDERED SYNTHETIC VINYL PATIENT EXAMINATION GLOVES, YELLOW 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.

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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