BK231004- Blood Product Questionnaire Module
510(k) Number: BK231004
Applicant: Buoy Software, LLC
Device Name: Blood Product Questionnaire Module
Decision Date: 11/16/2023
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: BK231004
Applicant: Buoy Software, LLC
Device Name: Blood Product Questionnaire Module
Decision Date: 11/16/2023