510(k) K130794

CELLTRACKS ANALYZER II SYSTEM by Veridex, LLC — Product Code NQI

K130794 is an FDA 510(k) premarket notification submitted by Veridex, LLC for the device "CELLTRACKS ANALYZER II SYSTEM". The FDA issued a decision of Substantially Equivalent on June 20, 2013. The device falls under product code NQI (System, Immunomagnetic, Circulating Cancer Cell, Enumeration), a Class II device regulated under 21 CFR 866.6020. Veridex, LLC has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 20, 2013
Date Received
March 22, 2013
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, Immunomagnetic, Circulating Cancer Cell, Enumeration
Device Class
Class II
Regulation Number
866.6020
Review Panel
PA
Submission Type

In vitro diagnostic device to aid in the enumeration of immunomagnetically selected and fluorescently identified circulating tumor cells of epithelial origin in whole blood for prediction of cancer progression and survival.