| K-number | K241607 |
| Device name | MyoStrain (6.0) |
| Applicant | Myocardial Solutions, Inc. |
| Product code | LNH |
| Device class | Class II |
| Decision date | Aug 26, 2024 |
| Decision | Substantially Equivalent |
| Regulation | 892.1000 |
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