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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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