Philips Ultrasound, Inc. · Class II · Cleared Jul 17, 2009
| K-number | K091804 |
| Device name | CX50 VERSION 2.0 DIAGNOSTIC ULTRASOUND SYSTEM AND TRANSDUCERS |
| Applicant | Philips Ultrasound, Inc. |
| Product code | ITX |
| Device class | Class II |
| Decision date | Jul 17, 2009 |
| Decision | Substantially Equivalent |
| Regulation | 892.1570 |
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