BK230804 - Elecsys HIV Duo
510(k) Number: BK230804
Applicant: Roche Diagnostics
Device Name: Elecsys HIV Duo
Decision Date: 4/4/2023
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: BK230804
Applicant: Roche Diagnostics
Device Name: Elecsys HIV Duo
Decision Date: 4/4/2023