Vasca, Inc. · Class II · Cleared Dec 4, 2003
| K-number | K023023 |
| Device name | LIFESITE HEMODIALYSIS ACCESS SYSTEM, CANNULA EXCHANGE KIT, INSERTION KIT, ACCESS CANNILA |
| Applicant | Vasca, Inc. |
| Product code | MSD |
| Device class | Class II |
| Decision date | Dec 4, 2003 |
| Decision | Substantially Equivalent |
| Regulation | 876.5540 |
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