Device |
reagent red blood cells |
Regulation Description |
Reagent Red Blood Cells. |
Definition |
For the detection of or identification of human blood-group antibodies |
Physical State |
Sourced from human blood |
Technical Method |
Antigen and antibody reaction by hemagglutination, column agglutination (gel technique), solid phase or microplate |
Target Area |
Serum or plasma |
Regulation Medical Specialty |
Hematology |
Review Panel |
Hematology |
Product Code | QHT |
Premarket Review |
Center for Biologics Evaluation & Research (CBER)
|
Unclassified Reason
|
Pre-Amendment
|
Submission Type |
Contact ODE
|
Regulation Number |
660.30
|
Device Class |
Unclassified
|
Total Product Life Cycle (TPLC) |
TPLC Product Code Report
|
GMP Exempt? |
No
|
Summary Malfunction Reporting |
Ineligible |
Implanted Device? |
No
|
Life-Sustain/Support Device? |
No
|
Third Party Review |
Not Third Party Eligible |
|
|