Philips Medical Systems Nederland B.V. · Class II · Cleared Dec 2, 2016
| K-number | K162859 |
| Device name | Allura Xper FD series and Allura Xper OR Table series |
| Applicant | Philips Medical Systems Nederland B.V. |
| Product code | OWB |
| Device class | Class II |
| Decision date | Dec 2, 2016 |
| Decision | Substantially Equivalent |
| Regulation | 892.1650 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov