Konica Minolta Healthcare Americas, Inc.
FDA 510(k) & PMA Approved Devices — 6 products
Total Devices6
Categories3
Latest FDA decision2026-06-12
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K252996 | Universal 1417PI | MQB | 2026-06-12 | View |
| 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 |
No matching devices.