POWDER-FREE-VINYL EXAMINATION GLOVES, COLOR: WHITE
K-Number: K021353 · 2002-06-06
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Device Summary
Frequently Asked Questions
What is the POWDER-FREE-VINYL EXAMINATION GLOVES, COLOR: WHITE?
POWDER-FREE-VINYL EXAMINATION GLOVES, COLOR: WHITE is a medical device that received FDA 510(k) clearance on 2002-06-06. The listed applicant is Glormed Intl., Inc.. The 510(k) number is K021353.
When did POWDER-FREE-VINYL EXAMINATION GLOVES, COLOR: WHITE receive FDA 510(k) clearance?
POWDER-FREE-VINYL EXAMINATION GLOVES, COLOR: WHITE received FDA 510(k) clearance on 2002-06-06, under 510(k) number K021353.
Who is the listed applicant for POWDER-FREE-VINYL EXAMINATION GLOVES, COLOR: WHITE?
The FDA 510(k) record lists Glormed Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for POWDER-FREE-VINYL EXAMINATION GLOVES, COLOR: WHITE?
The FDA product code for POWDER-FREE-VINYL EXAMINATION GLOVES, COLOR: 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 Glormed 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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