PRE-POWDERED, NON-STERILE, VINYL EXAM GLOVES, YELLOW
K-Number: K032792 · 2003-10-15
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Device Summary
Frequently Asked Questions
What is the PRE-POWDERED, NON-STERILE, VINYL EXAM GLOVES, YELLOW?
PRE-POWDERED, NON-STERILE, VINYL EXAM GLOVES, YELLOW is a medical device that received FDA 510(k) clearance on 2003-10-15. The listed applicant is Shanghai Jiawang Industrial Co. , Ltd.. The 510(k) number is K032792.
When did PRE-POWDERED, NON-STERILE, VINYL EXAM GLOVES, YELLOW receive FDA 510(k) clearance?
PRE-POWDERED, NON-STERILE, VINYL EXAM GLOVES, YELLOW received FDA 510(k) clearance on 2003-10-15, under 510(k) number K032792.
Who is the listed applicant for PRE-POWDERED, NON-STERILE, VINYL EXAM GLOVES, YELLOW?
The FDA 510(k) record lists Shanghai Jiawang Industrial Co. , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PRE-POWDERED, NON-STERILE, VINYL EXAM GLOVES, YELLOW?
The FDA product code for PRE-POWDERED, NON-STERILE, VINYL EXAM 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.
Other records listing Shanghai Jiawang Industrial Co. , Ltd. 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
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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