LOW PROTEIN POWDER FREE LATEX EXAMINATION GLOVES
K-Number: K974782 · 1998-02-24
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Device Summary
Frequently Asked Questions
What is the LOW PROTEIN POWDER FREE LATEX EXAMINATION GLOVES?
LOW PROTEIN POWDER FREE LATEX EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1998-02-24. The listed applicant is Mexpo Intl., Inc.. The 510(k) number is K974782.
When did LOW PROTEIN POWDER FREE LATEX EXAMINATION GLOVES receive FDA 510(k) clearance?
LOW PROTEIN POWDER FREE LATEX EXAMINATION GLOVES received FDA 510(k) clearance on 1998-02-24, under 510(k) number K974782.
Who is the listed applicant for LOW PROTEIN POWDER FREE LATEX EXAMINATION GLOVES?
The FDA 510(k) record lists Mexpo Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LOW PROTEIN POWDER FREE LATEX EXAMINATION GLOVES?
The FDA product code for LOW PROTEIN POWDER FREE LATEX EXAMINATION GLOVES is LYY.
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 Mexpo 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: LYY)
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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