| K-number | K201908 |
| Device name | LIAISON Testosterone xt |
| Applicant | DiaSorin, Inc. |
| Product code | CDZ |
| Device class | Class I |
| Decision date | Oct 15, 2020 |
| Decision | Substantially Equivalent |
| Regulation | 862.1680 |
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