POWDER FREE VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED)
K-Number: K092109 · 2009-10-09
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Device Summary
Frequently Asked Questions
What is the POWDER FREE VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED)?
POWDER FREE VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED) is a medical device that received FDA 510(k) clearance on 2009-10-09. The listed applicant is Zhangjiangang All Fine Rubber-Plastic Products Co.. The 510(k) number is K092109.
When did POWDER FREE VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED) receive FDA 510(k) clearance?
POWDER FREE VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED) received FDA 510(k) clearance on 2009-10-09, under 510(k) number K092109.
Who is the listed applicant for POWDER FREE VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED)?
The FDA 510(k) record lists Zhangjiangang All Fine Rubber-Plastic Products Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for POWDER FREE VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED)?
The FDA product code for POWDER FREE VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED) 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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