| K-number | K222262 |
| Device name | Sunrise |
| Applicant | Sunrise SA |
| Product code | QRS |
| Device class | Class II |
| Decision date | Dec 22, 2022 |
| Decision | Substantially Equivalent |
| Regulation | 868.2376 |
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