Cordis Europa, N.V. · Class II · Cleared May 16, 2007
| K-number | K071189 |
| Device name | CORDIS AVIATOR PLUS PTA BALLOON DILATATION CATHETER |
| Applicant | Cordis Europa, N.V. |
| Product code | LIT |
| Device class | Class II |
| Decision date | May 16, 2007 |
| Decision | Substantially Equivalent |
| Regulation | 870.1250 |
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