Atlas FDA

CELLTRACKA ANALYZER II

FDA 510(k) clearance K050145 · decided 2005-03-15

Clearance details

K-number
K050145
Device name
CELLTRACKA ANALYZER II
Applicant
Immunicon Corp.
Decision
Substantially Equivalent
Date received
2005-01-24
Decision date
2005-03-15
Days to decision
50 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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CELLTRACKS ANALYZER II SYSTEM (K130794)Veridex, LLC2013-06-20
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Recalls involving this device

RecordFirmDate
CELLTRACKS ANALYZER II (Product Code 9555) Product Usage: The CELLTRACKS ANALYZER II is a recall (Z-1195-2014)Veridex, LLC2014-03-13
CellTracks Analyzer II. A semi-automated fluorescence microscope used to enumerate fluores recall (Z-1004-2012)Veridex, LLC2012-02-13