Diagnostic Products Corporation · Class II · Cleared Dec 22, 2006
| K-number | K063057 |
| Device name | IMMULITE/IMMULITE 1000, IMMULITE 2000 HIGH SENSITIVITY CRP |
| Applicant | Diagnostic Products Corporation |
| Product code | NQD |
| Device class | Class II |
| Decision date | Dec 22, 2006 |
| Decision | Substantially Equivalent |
| Regulation | 866.5270 |
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