ILLUMIGENE C. DIFFICILE, AND ILLUMIPRO-10
K-Number: K110012 · 2011-02-24
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Device Summary
Frequently Asked Questions
What is the ILLUMIGENE C. DIFFICILE, AND ILLUMIPRO-10?
ILLUMIGENE C. DIFFICILE, AND ILLUMIPRO-10 is a medical device that received FDA 510(k) clearance on 2011-02-24. The listed applicant is Meridian Bioscience, Inc.. The 510(k) number is K110012.
When did ILLUMIGENE C. DIFFICILE, AND ILLUMIPRO-10 receive FDA 510(k) clearance?
ILLUMIGENE C. DIFFICILE, AND ILLUMIPRO-10 received FDA 510(k) clearance on 2011-02-24, under 510(k) number K110012.
Who is the listed applicant for ILLUMIGENE C. DIFFICILE, AND ILLUMIPRO-10?
The FDA 510(k) record lists Meridian Bioscience, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ILLUMIGENE C. DIFFICILE, AND ILLUMIPRO-10?
The FDA product code for ILLUMIGENE C. DIFFICILE, AND ILLUMIPRO-10 is OMN.
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 Meridian Bioscience, 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: OMN)
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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