BK230843 - Reveos Automated Whole Blood Processing System
510(k) Number: BK230843
Applicant: Terumo BCT
Device Name: Reveos® Automated Whole Blood Processing System
Decision Date: 7/27/2023
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: BK230843
Applicant: Terumo BCT
Device Name: Reveos® Automated Whole Blood Processing System
Decision Date: 7/27/2023