Bayer Corp. · Class II · Cleared Aug 2, 1996
| K-number | K955760 |
| Device name | TOXOPLASMA IGG IN-VITRO DIAGNOSTIC SYSTEM |
| Applicant | Bayer Corp. |
| Product code | LGD |
| Device class | Class II |
| Decision date | Aug 2, 1996 |
| Decision | Substantially Equivalent |
| Regulation | 866.3780 |
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