GLOVEX LATEX EXAMINATION GLOVES
K-Number: K900561 · 1990-02-13
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Device Summary
Frequently Asked Questions
What is the GLOVEX LATEX EXAMINATION GLOVES?
GLOVEX LATEX EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1990-02-13. The listed applicant is Medical Latex Corp.. The 510(k) number is K900561.
When did GLOVEX LATEX EXAMINATION GLOVES receive FDA 510(k) clearance?
GLOVEX LATEX EXAMINATION GLOVES received FDA 510(k) clearance on 1990-02-13, under 510(k) number K900561.
Who is the listed applicant for GLOVEX LATEX EXAMINATION GLOVES?
The FDA 510(k) record lists Medical Latex Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GLOVEX LATEX EXAMINATION GLOVES?
The FDA product code for GLOVEX 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 Medical Latex Corp. 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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