| Device |
quality control for molecular immunohematology tests |
| Regulation Description |
Quality control kit for blood banking reagents. |
| Definition |
The quality control for molecular immunohematology assay is used to demonstrate that the test can correctly detect genetic variations of human erythrocyte antigens. |
| Physical State |
DNA or synthetic plasmids |
| Technical Method |
Molecular |
| Target Area |
N/A |
| Regulation Medical Specialty |
Hematology |
| Review Panel |
Pathology |
| Product Code | PFK |
| Premarket Review |
Center for Biologics Evaluation and Research Branch
(CBER)
CBER Division
(CBER)
|
| Submission Type |
510(k)
|
| Regulation Number |
864.9650
|
| Device Class |
2
|
| Total Product Life Cycle (TPLC) |
TPLC Product Code Report
|
| GMP Exempt? |
No
|
Summary Malfunction Reporting |
Eligible |
| Implanted Device? |
No
|
| Life-Sustain/Support Device? |
No
|
|
Third Party Review
|
Accredited Persons
|