DISPOSABLE POWDERED VINYL EXAM GLOVES
K-Number: K032190 · 2003-08-14
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Device Summary
Frequently Asked Questions
What is the DISPOSABLE POWDERED VINYL EXAM GLOVES?
DISPOSABLE POWDERED VINYL EXAM GLOVES is a medical device that received FDA 510(k) clearance on 2003-08-14. The listed applicant is Synmertex Co, Ltd.. The 510(k) number is K032190.
When did DISPOSABLE POWDERED VINYL EXAM GLOVES receive FDA 510(k) clearance?
DISPOSABLE POWDERED VINYL EXAM GLOVES received FDA 510(k) clearance on 2003-08-14, under 510(k) number K032190.
Who is the listed applicant for DISPOSABLE POWDERED VINYL EXAM GLOVES?
The FDA 510(k) record lists Synmertex Co, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DISPOSABLE POWDERED VINYL EXAM GLOVES?
The FDA product code for DISPOSABLE POWDERED VINYL EXAM GLOVES 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 Synmertex 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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