FDA 510(k) Applications Submitted by Konica Minolta Healthcare Americas, Inc

FDA 510(k) Number Submission Date Device Name Applicant
K221853 06/27/2022 OTC DDR Konica Minolta Healthcare Americas, Inc
K193225 11/22/2019 KDR AU-DDR System Advanced U-Arm with Dynamic Digital Radiography, KDR AU System Advanced U-Arm with Static Digital Radiography Konica Minolta Healthcare Americas, Inc
K214012 12/22/2021 Straight Arm DDR Konica Minolta Healthcare Americas, Inc


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