K171716 is an FDA 510(k) clearance for the SKR 3000. This device is classified as a Solid State X-ray Imager (flat Panel/digital Imager) (Class II - Special Controls, product code MQB).
Submitted by Konica Minolta, Inc. (Hino-Shi, JP). The FDA issued a Cleared decision on August 25, 2017, 77 days after receiving the submission on June 9, 2017.
This device falls under the Radiology FDA review panel. Regulated under 21 CFR 892.1680.
| 510(k) Number | K171716 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | June 09, 2017 |
| Decision Date | August 25, 2017 |
| Days to Decision | 77 days |
| Submission Type | Traditional |
| Review Panel | Radiology (RA) |
| Summary | Statement |
| Product Code | MQB — Solid State X-ray Imager (flat Panel/digital Imager) |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 892.1680 |