| K-number | K202922 |
| Device name | END 200 Endoscopic Tubeset |
| Applicant | Palliare , Ltd. |
| Product code | FCX |
| Device class | Class II |
| Decision date | Jul 8, 2021 |
| Decision | Substantially Equivalent |
| Regulation | 876.1500 |
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