Jeil Tech Co., Ltd. · Class II · Cleared Sep 19, 2022
| K-number | K213013 |
| Device name | Sterile Single-use LDV Syringe, CHOICARE Sterile Single-use LDV Syringe |
| Applicant | Jeil Tech Co., Ltd. |
| Product code | QNQ |
| Device class | Class II |
| Decision date | Sep 19, 2022 |
| Decision | Substantially Equivalent |
| Regulation | 880.5860 |
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