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Array Corp.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K063424
FILM DIGITZER, MODEL 2908 MAMMO PRO
December 21, 2006
K033637
MEDICAL IMAGE DIGITIZER, MODEL 2908
December 17, 2003
K982785
FILM DIGITIZER MODEL 2905
October 15, 1998