Immunicon Corp. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Immunicon Corp. has 6 FDA 510(k) cleared medical devices. Based in Huntingdon Valley, US.
Historical record: 6 cleared submissions from 2002 to 2006. Primary specialty: Hematology.
Browse the FDA 510(k) cleared devices submitted by Immunicon Corp. Filter by specialty or product code using the sidebar.
6 devices
Cleared
Mar 16, 2006
CELLTRACKS ANALYZER II
Pathology
58d
Cleared
Mar 15, 2005
CELLTRACKA ANALYZER II
Pathology
50d
Cleared
Mar 12, 2004
IMMUNICON CELLTRACKS AUTOPREP SYSTEM
Hematology
58d
Cleared
Nov 24, 2003
IMMUNICON CELLTRACKS ANALYZER
Hematology
301d
Cleared
Aug 08, 2003
IMMUNICON CELLSAVE PRESERVATIVE TUBE
Chemistry
164d
Cleared
Sep 30, 2002
CELLPREP SAMPLE PREPARATION SYSTEM, MODEL 9518
Hematology
62d