Abk Biomedical, Inc. · Class II · Cleared Feb 13, 2024
| K-number | K234123 |
| Device name | Easi-Vue® embolic microspheres System |
| Applicant | Abk Biomedical, Inc. |
| Product code | KRD |
| Device class | Class II |
| Decision date | Feb 13, 2024 |
| Decision | Substantially Equivalent |
| Regulation | 870.3300 |
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