Vygon USA · Class II · Cleared Nov 2, 2018
| K-number | K181208 |
| Device name | Vygon Midline 3 Fr SL Catheter; Vygon Midline 4 Fr SL Catheter; Vygon Midline 5 Fr DL Catheter |
| Applicant | Vygon USA |
| Product code | PND |
| Device class | Class II |
| Decision date | Nov 2, 2018 |
| Decision | Substantially Equivalent |
| Regulation | 880.5200 |
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