BK241136 - Lookback Notification System version 2.0
510(k) Number: BK241136
Applicant: BioLife Plasma Services LP
Device Name: Lookback Notification System version 2.0
Decision Date: 2/20/2025
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: BK241136
Applicant: BioLife Plasma Services LP
Device Name: Lookback Notification System version 2.0
Decision Date: 2/20/2025