Device Type ID | 2296 |
Device Name | Fluid, Diluting, Red-cell |
Regulation Description | Blood Cell Diluent. |
Regulation Medical Specialty | Hematology |
Review Panel | Hematology |
Premarket Review | Office Of In Vitro Diagnostics And Radiological Health (OIR) |
Submission Type | 510(K) Exempt |
CFR Regulation Number | 864.8200 [🔎] |
FDA Device Classification | Class 1 Medical Device |
Product Code | GJN |
GMP Exempt | No |
Summary MR | Eligible |
Implanted Device | No |
Life Support Device | No |
Third Party Review | Not Third Party Eligible |
Device Type ID | 2296 |
Device | Fluid, Diluting, Red-cell |
Product Code | GJN |
FDA Device Classification | Class 1 Medical Device |
Regulation Description | Blood Cell Diluent. |
CFR Regulation Number | 864.8200 [🔎] |