ClearanceBrief
Company ยท US

Immunicon Corp.

FDA 510(k) clearances and medical device recalls filed under this name, 2002 to 2006. Name variants (Inc, Corp, punctuation) are merged.

6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
GKHApparatus, Automated Blood Cell Diluting2
NQISystem, Immunomagnetic, Circulating Cancer Cell, Enumeration2
GKZCounter, Differential Cell1
JKATubes, Vials, Systems, Serum Separators, Blood Collection1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Mar 16, 2006K060110CELLTRACKS ANALYZER II
Immunicon Corp.
NQI
Mar 15, 2005K050145CELLTRACKA ANALYZER II
Immunicon Corp.
NQI
Mar 12, 2004K040077IMMUNICON CELLTRACKS AUTOPREP SYSTEM
Immunicon Corp.
GKH
Nov 24, 2003K030263IMMUNICON CELLTRACKS ANALYZER
Immunicon Corp.
GKZ
Aug 8, 2003K030596IMMUNICON CELLSAVE PRESERVATIVE TUBE
Immunicon Corp.
JKA
Sep 30, 2002K022512CELLPREP SAMPLE PREPARATION SYSTEM, MODEL 9518
Immunicon Corp.
GKH

Latest recalls

DateFirm and productCodeLinked 510(k)
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