| K-number | K895421 |
| Device name | CORTISOL TEST SYSTEM |
| Applicant | Baxter Healthcare Corp |
| Product code | JFT |
| Device class | Class II |
| Decision date | Dec 7, 1989 |
| Decision | Substantially Equivalent |
| Regulation | 862.1205 |
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