BK231018 - AHC Platelet Concentrate Separator
510(k) Number: BK231018
Applicant: Sunphoria Co.,Ltd
Device Name: AHC Platelet Concentrate Separator
Decision Date: 1/10/2025
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: BK231018
Applicant: Sunphoria Co.,Ltd
Device Name: AHC Platelet Concentrate Separator
Decision Date: 1/10/2025