Device Type ID | 2327 |
Device Name | Cell Enzymes (erythrocytic And Leukocytic) |
Regulation Description | Red Blood Cell Enzyme Assay. |
Regulation Medical Specialty | Hematology |
Review Panel | Hematology |
Premarket Review | Office Of In Vitro Diagnostics And Radiological Health (OIR) |
Submission Type | 510(k) |
CFR Regulation Number | 864.7100 [🔎] |
FDA Device Classification | Class 2 Medical Device |
Product Code | JBE |
GMP Exempt | No |
Summary MR | Eligible |
Implanted Device | No |
Life Support Device | No |
Third Party Review | Eligible For Accredited Persons Expansion Pilot Program |