Coloplast · Class II · Cleared Jul 26, 2024
| K-number | K241028 |
| Device name | Luja female (20051); Luja female (20052); Luja female (20054); Luja female (20056) |
| Applicant | Coloplast |
| Product code | EZD |
| Device class | Class II |
| Decision date | Jul 26, 2024 |
| Decision | Substantially Equivalent |
| Regulation | 876.5130 |
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