BK230820 - Erytra Eflexis
510(k) Number: BK230820
Applicant: Diagnostic Grifols, S.A.
Device Name: Erytra Eflexis
Decision Date: 6/22/2023
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: BK230820
Applicant: Diagnostic Grifols, S.A.
Device Name: Erytra Eflexis
Decision Date: 6/22/2023