| K-number | K896162 |
| Device name | ABBOTT IMX PROLACTIN |
| Applicant | Abbott Laboratories |
| Product code | CFT |
| Device class | Class I |
| Decision date | Jan 19, 1990 |
| Decision | Substantially Equivalent |
| Regulation | 862.1625 |
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