LANEX EXAM GLOVES
K-Number: K910977 · 1991-04-12
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Device Summary
Frequently Asked Questions
What is the LANEX EXAM GLOVES?
LANEX EXAM GLOVES is a medical device that received FDA 510(k) clearance on 1991-04-12. The listed applicant is Multi M Intl., Inc.. The 510(k) number is K910977.
When did LANEX EXAM GLOVES receive FDA 510(k) clearance?
LANEX EXAM GLOVES received FDA 510(k) clearance on 1991-04-12, under 510(k) number K910977.
Who is the listed applicant for LANEX EXAM GLOVES?
The FDA 510(k) record lists Multi M Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LANEX EXAM GLOVES?
The FDA product code for LANEX EXAM 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 Multi M 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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