Ureteral Stent Company · Class II · Cleared Mar 22, 2024
| K-number | K232920 |
| Device name | RELIEF Ureteral Stent Kit; Model: RS-001 - 6 Fr x 24cm, RELIEF Ureteral Stent Kit; Model: RS-002 - 6 Fr x 26cm |
| Applicant | Ureteral Stent Company |
| Product code | FAD |
| Device class | Class II |
| Decision date | Mar 22, 2024 |
| Decision | Substantially Equivalent |
| Regulation | 876.4620 |
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