Centers for Disease Control and Prevention · Class II · Cleared Sep 8, 1981
| K-number | K812007 |
| Device name | LEGIONELLA INDIRECT FLUOR. ANTIBODY |
| Applicant | Centers for Disease Control and Prevention |
| Product code | LHL |
| Device class | Class II |
| Decision date | Sep 8, 1981 |
| Decision | Substantially Equivalent |
| Regulation | 866.3300 |
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