| K-number | K222881 |
| Device name | Access hsTnI |
| Applicant | Beckman Coulter, Inc. |
| Product code | MMI |
| Device class | Class II |
| Decision date | Dec 18, 2023 |
| Decision | Substantially Equivalent |
| Regulation | 862.1215 |
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