| K-number | K152826 |
| Device name | NoCord |
| Applicant | Centrix, Inc. |
| Product code | ELW |
| Device class | Class II |
| Decision date | May 27, 2016 |
| Decision | Substantially Equivalent |
| Regulation | 872.3660 |
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