BK230811 - Blood Typing Manager, version 3.0
510(k) Number: BK230811
Applicant: Diagnostic Grifols, S. A.
Device Name: Blood Typing Manager, version 3.0
Decision Date: 7/24/2023
On Oct. 1, 2024, the FDA began implementing a reorganization impacting many parts of the agency. We are in the process of updating FDA.gov content to reflect these changes.
510(k) Number: BK230811
Applicant: Diagnostic Grifols, S. A.
Device Name: Blood Typing Manager, version 3.0
Decision Date: 7/24/2023