Cardica, Inc. · Class II · Cleared Jun 25, 2010
| K-number | K101018 |
| Device name | CARDICA C-PORT XA PLUS DISTAL ANASTOMOSIS SYSTEM, MODEL FG-000100 |
| Applicant | Cardica, Inc. |
| Product code | FZP |
| Device class | Class II |
| Decision date | Jun 25, 2010 |
| Decision | Substantially Equivalent |
| Regulation | 878.4300 |
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