BK230814 - SmartDMS
510(k) Number: BK230814
Applicant: Life Plasma, Inc.
Device Name: SmartDMS
Decision Date: 4/16/2024
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: BK230814
Applicant: Life Plasma, Inc.
Device Name: SmartDMS
Decision Date: 4/16/2024