Philips Health Care · Class II · Cleared Oct 4, 2017
| K-number | K172607 |
| Device name | Philips EPIQ 5 Diagnostic Ultrasound System, EPIQ 7 Diagnostic Ultrasound System, Affiniti 30 Diagnostic Ultrasound System, Affiniti 50 Diagnostic Ultrasound System, Affiniti 70 Diagnostic Ultrasound System |
| Applicant | Philips Health Care |
| Product code | IYN |
| Device class | Class II |
| Decision date | Oct 4, 2017 |
| Decision | Substantially Equivalent |
| Regulation | 892.1550 |
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