Philips Medical Systems Nederland B.V. · Class II · Cleared May 21, 2013
| K-number | K130842 |
| Device name | ALLURA XPER FD OR TABLE SERIES; ALLURA XPER FD10 SERIES; ALLURA XPER FD20 SERIES; ALLURA XPER FD BIPLANE SERIES |
| Applicant | Philips Medical Systems Nederland B.V. |
| Product code | IZI |
| Device class | Class II |
| Decision date | May 21, 2013 |
| Decision | Substantially Equivalent |
| Regulation | 892.1600 |
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