Reference Diagnostics, Inc. · Class I · Cleared Jan 28, 1999
| K-number | K984107 |
| Device name | RDI DIRECT LDL CHOLESTEROL TEST |
| Applicant | Reference Diagnostics, Inc. |
| Product code | MRR |
| Device class | Class I |
| Decision date | Jan 28, 1999 |
| Decision | Substantially Equivalent |
| Regulation | 862.1475 |
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