K171719 is an FDA 510(k) clearance for the Hybrid3D. This device is classified as a System, Tomography, Computed, Emission (Class II - Special Controls, product code KPS).
Submitted by Hermes Medical Solutions AB (Stockholm, SE). The FDA issued a Cleared decision on November 21, 2017, 165 days after receiving the submission on June 9, 2017.
This device falls under the Radiology FDA review panel. Regulated under 21 CFR 892.1200.
| 510(k) Number | K171719 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | June 09, 2017 |
| Decision Date | November 21, 2017 |
| Days to Decision | 165 days |
| Submission Type | Traditional |
| Review Panel | Radiology (RA) |
| Summary | Summary PDF |
| Product Code | KPS - System, Tomography, Computed, Emission |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 892.1200 |