Shenzhen Kaiyan Medical CO , Ltd. · Class II · Cleared Jul 21, 2021
| K-number | K203271 |
| Device name | Aduro light therapy Handheld |
| Applicant | Shenzhen Kaiyan Medical CO , Ltd. |
| Product code | OLP |
| Device class | Class II |
| Decision date | Jul 21, 2021 |
| Decision | Substantially Equivalent |
| Regulation | 878.4810 |
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