| K-number | K951541 |
| Device name | IMX RUBELLA IGG |
| Applicant | Abbott Laboratories |
| Product code | LFX |
| Device class | Class II |
| Decision date | Jul 16, 1996 |
| Decision | Substantially Equivalent |
| Regulation | 866.3510 |
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