Embol-X, Inc. · Class II · Cleared Sep 5, 2002
| K-number | K020693 |
| Device name | AORTIC CANNULA, METAL J-TIP (24FR) MODEL #CF00100; AORTIC CANNULA, PLASTIC J-TIP (24FR) MODEL #CF00101 |
| Applicant | Embol-X, Inc. |
| Product code | DWF |
| Device class | Class II |
| Decision date | Sep 5, 2002 |
| Decision | Substantially Equivalent |
| Regulation | 870.4210 |
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