Bayer Corp. · Class II · Cleared Jun 9, 1995
| K-number | K951631 |
| Device name | DIGOXIN ASSAY FOR THE TECCHNICON RA/OPERA SYSTEMS IN-VITRO DIAGNOSTIC SYSTEMS |
| Applicant | Bayer Corp. |
| Product code | LFM |
| Device class | Class II |
| Decision date | Jun 9, 1995 |
| Decision | Substantially Equivalent |
| Regulation | 862.3300 |
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