BK241132 - Elecsys Syphilis, Elecsys Anti-CMV, cobas pro serology solution
510(k) Number: BK241132
Applicant: Roche Diagnostics
Device Name: Elecsys Syphilis, Elecsys Anti-CMV, cobas pro serology solution
Decision Date: 11/6/2024
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: BK241132
Applicant: Roche Diagnostics
Device Name: Elecsys Syphilis, Elecsys Anti-CMV, cobas pro serology solution
Decision Date: 11/6/2024