Ortho Diagnostic Systems, Inc. · Class I · Cleared Jan 4, 1989
| K-number | K883940 |
| Device name | ORTHO* ROTAVIRUS LATEX AGGLUTINATION TEST |
| Applicant | Ortho Diagnostic Systems, Inc. |
| Product code | LIQ |
| Device class | Class I |
| Decision date | Jan 4, 1989 |
| Decision | Substantially Equivalent |
| Regulation | 866.3405 |
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