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Konica Minolta Healthcare Americas, Inc.

FDA 510(k) & PMA Approved Devices — 5 products

Total Devices5
Categories3
Latest Approval2022-07-27
TypeNumberDevice NameCodeDate
510(k) K221853 OTC DDR KPR 2022-07-27 View
510(k) K214030 Universal DR 1748 MQB 2022-01-21 View
510(k) K214012 Straight Arm DDR KPR 2022-01-12 View
510(k) K203743 EXA LLZ 2021-12-10 View
510(k) K193225 KDR AU-DDR System Advanced U-Arm with Dynamic Digital Radiography, KDR AU System Advanced U-Arm with Static Digital Radiography KPR 2020-01-15 View
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