| K-number | K935469 |
| Device name | SYNELISA DHEA-SULFATE |
| Applicant | Elias U.S.A., Inc. |
| Product code | JKC |
| Device class | Class I |
| Decision date | Mar 22, 1994 |
| Decision | Substantially Equivalent |
| Regulation | 862.1245 |
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