BK210652 - BD Stem Cell Enumeration Kit
510(k) Number: BK210652
Applicant: Becton, Dickinson and Company
Device Name: BD® Stem Cell Enumeration Kit
Decision Date: 1/27/2022
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: BK210652
Applicant: Becton, Dickinson and Company
Device Name: BD® Stem Cell Enumeration Kit
Decision Date: 1/27/2022