Device Type ID | 4913 |
Device Name | Igd, Peroxidase, Antigen, Antiserum, Control |
Regulation Description | Immunoglobulins A, G, M, D, And E Immunological Test System. |
Regulation Medical Specialty | Immunology |
Review Panel | Pathology |
Premarket Review | Office Of In Vitro Diagnostics And Radiological Health (OIR) |
Submission Type | 510(k) |
CFR Regulation Number | 866.5510 [🔎] |
FDA Device Classification | Class 2 Medical Device |
Product Code | DGH |
GMP Exempt | No |
Summary MR | Eligible |
Implanted Device | No |
Life Support Device | No |
Third Party Review | Eligible For Accredited Persons Program |