BK241075 - Atellica IM HIV Ag/Ab Combo (CHIV)
510(k) Number: BK241075
Applicant: Siemens Healthcare Diagnostics, Inc.
Device Name: Atellica® IM HIV Ag/Ab Combo (CHIV)
Decision Date: 11/7/2024
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: BK241075
Applicant: Siemens Healthcare Diagnostics, Inc.
Device Name: Atellica® IM HIV Ag/Ab Combo (CHIV)
Decision Date: 11/7/2024