BK231035 - Rika Plasma Donation System (V2.1)
510(k) Number: BK231035
Applicant: Terumo BCT
Device Name: Rika Plasma Donation System (V2.1)
Decision Date: 3/7/2024
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: BK231035
Applicant: Terumo BCT
Device Name: Rika Plasma Donation System (V2.1)
Decision Date: 3/7/2024