BROTHERS POWDERED SYNTHETIC VINYL PATIENT EXAMINATION GLOVES, YELLOW
K-Number: K032323 · 2003-10-07
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Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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