FDA 510(k) Applications Submitted by SHIGEYUKI KOJIMA

FDA 510(k) Number Submission Date Device Name Applicant
K121109 04/12/2012 AERODR X70 KONICA MINOLTA MEDICAL & GRAPHIC, INC.
K151060 04/20/2015 Ultrasound System SONIMAGE HS1 KONICA MINOLTA, INC.
K151465 06/01/2015 AeroDR SYSTEM 2 KONICA MINOLTA, INC.
K142197 08/11/2014 ULTRASOUND SYSTEM SONIMAGE HS1, LINEAR PROBE L18-4, CONVEX PROBE C5-2 KONICA MINOLTA INC.
K152577 09/09/2015 ULTRASOUND SYSTEM SONIMAGE HS 1 KONICA MINOLTA, INC.


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