BK220746 - Procleix WNV/Babesia Quality Control
510(k) Number: BK220746
Applicant: Grifols Diagnostic Solutions Inc.
Device Name: Procleix® WNV/Babesia Quality Control
Decision Date: 10/14/2022
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: BK220746
Applicant: Grifols Diagnostic Solutions Inc.
Device Name: Procleix® WNV/Babesia Quality Control
Decision Date: 10/14/2022