POWDERED VINYL EXAM GLOVES, WHITE
K-Number: K030927 · 2003-04-17
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Device Summary
Frequently Asked Questions
What is the POWDERED VINYL EXAM GLOVES, WHITE?
POWDERED VINYL EXAM GLOVES, WHITE is a medical device that received FDA 510(k) clearance on 2003-04-17. The listed applicant is Copioumed Intl., Inc.. The 510(k) number is K030927.
When did POWDERED VINYL EXAM GLOVES, WHITE receive FDA 510(k) clearance?
POWDERED VINYL EXAM GLOVES, WHITE received FDA 510(k) clearance on 2003-04-17, under 510(k) number K030927.
Who is the listed applicant for POWDERED VINYL EXAM GLOVES, WHITE?
The FDA 510(k) record lists Copioumed Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for POWDERED VINYL EXAM GLOVES, WHITE?
The FDA product code for POWDERED VINYL EXAM 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 Copioumed Intl., Inc. 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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