St Jude Medical · Class II · Cleared Mar 2, 2012
| K-number | K113584 |
| Device name | PRESSUREWIRE CERTUS, CERTUS 300, AERIS, AERIS 300, AND RECEIVER |
| Applicant | St Jude Medical |
| Product code | DXO |
| Device class | Class II |
| Decision date | Mar 2, 2012 |
| Decision | Substantially Equivalent |
| Regulation | 870.2870 |
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