| K-number | K123866 |
| Device name | TANYX |
| Applicant | Medecell Us, Inc. |
| Product code | NUH |
| Device class | Class II |
| Decision date | Sep 13, 2013 |
| Decision | Substantially Equivalent |
| Regulation | 882.5890 |
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