BK230961 - AQUIOS CL Flow Cytometer and AQUIOS Stem Kit
510(k) Number: BK230961
Applicant: Beckman Coulter, Inc.
Device Name: AQUIOS CL Flow Cytometer and AQUIOS Stem Kit
Decision Date: 9/1/2023
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: BK230961
Applicant: Beckman Coulter, Inc.
Device Name: AQUIOS CL Flow Cytometer and AQUIOS Stem Kit
Decision Date: 9/1/2023