K193225 is an FDA 510(k) clearance for the KDR AU-DDR System Advanced U-Arm with Dynamic Digital Radiography, KDR AU System Advanced U-Arm with Static Digital Radiography. This device is classified as a System, X-ray, Stationary (Class II - Special Controls, product code KPR).
Submitted by Konica Minolta Healthcare Americas, Inc. (Garner, US). The FDA issued a Cleared decision on January 15, 2020, 54 days after receiving the submission on November 22, 2019.
This device falls under the Radiology FDA review panel. Regulated under 21 CFR 892.1680.
| 510(k) Number | K193225 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | November 22, 2019 |
| Decision Date | January 15, 2020 |
| Days to Decision | 54 days |
| Submission Type | Traditional |
| Review Panel | Radiology (RA) |
| Summary | Summary PDF |
| Product Code | KPR - System, X-ray, Stationary |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 892.1680 |