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FDA 510(k)

ILLUMIGENE C. DIFFICILE, AND ILLUMIPRO-10

K-Number: K110012 · 2011-02-24

Decision Date2011-02-24
Product CodeOMN
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

ILLUMIGENE C. DIFFICILE, AND ILLUMIPRO-10 is the device name listed in this FDA 510(k) record. The listed applicant is Meridian Bioscience, Inc.. It received FDA 510(k) clearance on 2011-02-24 under 510(k) number K110012. The device is classified under product code OMN. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

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.

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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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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