| Device Type ID | 3222 |
| Device Name | Antigen, Indirect Fluorescent Antibody Test, Echinococcus Granulosus |
| Regulation Description | Echinococcus Spp. Serological Reagents. |
| Regulation Medical Specialty | Microbiology |
| Review Panel | Microbiology |
| Premarket Review | Office Of In Vitro Diagnostics And Radiological Health (OIR)
|
| Submission Type | 510(K) Exempt |
| CFR Regulation Number | 866.3200 [🔎] |
| FDA Device Classification | Class 1 Medical Device |
| Product Code | GPD |
| GMP Exempt | No |
| Summary MR | Eligible |
| Implanted Device | No |
| Life Support Device | No |
| Third Party Review | Not Third Party Eligible |