Atlas FDA

CELLTRACKS ANALYZER II

FDA 510(k) clearance K060110 · decided 2006-03-16

Clearance details

K-number
K060110
Device name
CELLTRACKS ANALYZER II
Applicant
Immunicon Corp.
Decision
Substantially Equivalent
Date received
2006-01-17
Decision date
2006-03-16
Days to decision
58 days
Clearance type
Traditional
Product code
NQI
Device class
2
Regulation number
866.6020
Medical specialty
Immunology
Advisory committee
Immunology
Location
Huntingdon Valley, PA, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

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RecordFirmDate
CELLTRACKS ANALYZER II SYSTEM (K130794)Veridex, LLC2013-06-20
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CELLSEARCH CIRCULATING TUMOR CELL KIT (K073338)Veridex, LLC2008-02-26
CELLSEARCH CIRCULATING TUMOR CELL KIT (K071729)Veridex, LLC2007-11-20
CELLSEARCH CIRCULATING TUMOR CELL KIT (K062013)Veridex, LLC2006-12-14
MODIFICATION TO CELLSEARCH CIRCULATING TUMOR CELL KIT (K052191)Veridex, LLC2005-10-27
CELLTRACKA ANALYZER II (K050145)Immunicon Corp.2005-03-15
CELLSEARCH CIRCULATING TUMOR CELL KIT (K050245)Veridex, LLC2005-03-15
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Recalls involving this device

RecordFirmDate
CellTracks Analyzer II. A semi-automated fluorescence microscope used to enumerate fluores recall (Z-1004-2012)Veridex, LLC2012-02-13