| K-number | K241365 |
| Device name | Pixie Pulse (SM9068) |
| Applicant | Pixie Cup, LLC |
| Product code | NUH |
| Device class | Class II |
| Decision date | Aug 12, 2024 |
| Decision | Substantially Equivalent |
| Regulation | 882.5890 |
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