BK230980 - BD Vacutainer K2EDTA Blood Collection Tubes
510(k) Number: BK230980
Applicant: Becton, Dickinson & Company
Device Name: BD Vacutainer® K2EDTA Blood Collection Tubes
Decision Date: 4/17/2024
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: BK230980
Applicant: Becton, Dickinson & Company
Device Name: BD Vacutainer® K2EDTA Blood Collection Tubes
Decision Date: 4/17/2024