CELLTRACKS AUTOPREP SYSTEM
K-Number: K110406 · 2012-01-20
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Device Summary
Frequently Asked Questions
What is the CELLTRACKS AUTOPREP SYSTEM?
CELLTRACKS AUTOPREP SYSTEM is a medical device that received FDA 510(k) clearance on 2012-01-20. The listed applicant is Veridex, LLC. The 510(k) number is K110406.
When did CELLTRACKS AUTOPREP SYSTEM receive FDA 510(k) clearance?
CELLTRACKS AUTOPREP SYSTEM received FDA 510(k) clearance on 2012-01-20, under 510(k) number K110406.
Who is the listed applicant for CELLTRACKS AUTOPREP SYSTEM?
The FDA 510(k) record lists Veridex, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CELLTRACKS AUTOPREP SYSTEM?
The FDA product code for CELLTRACKS AUTOPREP SYSTEM is NQI.
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 Veridex, LLC 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: NQI)
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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