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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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