FDA 510(k) Applications Submitted by CARIDIANBCT, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K103090 10/19/2010 SPECTRA OPTIA R APHERESIS SYSTEM CARIDIANBCT, INC.
K113480 11/23/2011 SPECTRA OPTIA APHERESIS SYSTEM CARIDIANBCT, INC.


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