Bayer Corp. · Class II · Cleared Apr 15, 1996
| K-number | K951359 |
| Device name | RUBELLA IGG ASSAY FOR THE TECHNICON IMMUNO 1 SYSTEM IN-VITRO DIAGNOSTIC DEVICE |
| Applicant | Bayer Corp. |
| Product code | LFX |
| Device class | Class II |
| Decision date | Apr 15, 1996 |
| Decision | Substantially Equivalent |
| Regulation | 866.3510 |
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