Baxter Healthcare Corp · Class I · Cleared Jun 12, 1990
| K-number | K901673 |
| Device name | PROLACTIN (LACTOGEN) TEST SYSTEM |
| Applicant | Baxter Healthcare Corp |
| Product code | CFT |
| Device class | Class I |
| Decision date | Jun 12, 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