COBAS INTEGRA C 111
K-Number: K063744 · 2007-01-17
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Device Summary
Frequently Asked Questions
What is the COBAS INTEGRA C 111?
COBAS INTEGRA C 111 is a medical device that received FDA 510(k) clearance on 2007-01-17. The listed applicant is Rochdiag. The 510(k) number is K063744.
When did COBAS INTEGRA C 111 receive FDA 510(k) clearance?
COBAS INTEGRA C 111 received FDA 510(k) clearance on 2007-01-17, under 510(k) number K063744.
Who is the listed applicant for COBAS INTEGRA C 111?
The FDA 510(k) record lists Rochdiag as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for COBAS INTEGRA C 111?
The FDA product code for COBAS INTEGRA C 111 is CIG.
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 Rochdiag 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: CIG)
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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