BK241062 - BloodTrack Software 4.16.0
510(k) Number: BK241062
Applicant: Haemonetics Corporation
Device Name: BloodTrack Software 4.16.0
Decision Date: 6/21/2024
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: BK241062
Applicant: Haemonetics Corporation
Device Name: BloodTrack Software 4.16.0
Decision Date: 6/21/2024