Bayer Corp. · Class II · Cleared Aug 29, 1997
| K-number | K971998 |
| Device name | ADVIA 120 HEMATOLOGY SYSTEM, IN VITRO DIAGNOSTIC SYSTEM |
| Applicant | Bayer Corp. |
| Product code | GKL |
| Device class | Class II |
| Decision date | Aug 29, 1997 |
| Decision | Substantially Equivalent |
| Regulation | 864.5200 |
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