FDA 510(k) Applications Submitted by KONICA MINOLTA SENSING, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K010413 02/12/2001 MINOLTA PULSOX-3SI, PULSOX-3IA, PULSOX-3LI KONICA MINOLTA SENSING, INC.
K021469 05/07/2002 MINOLTA PULSOX-2 KONICA MINOLTA SENSING, INC.
K053419 12/08/2005 KONICA MINOLTA PULSOX-300, 300I KONICA MINOLTA SENSING, INC.


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