ADVIA Centaur BR— 510(k) K193489
Substantially EquivalentSiemens Healthcare Diagnostics, Inc.
FDA 510(k) clearance K193489 for ADVIA Centaur BR, Substantially Equivalent on 2020-02-13. Applicant: Siemens Healthcare Diagnostics, Inc..
Clearance details
- Applicant
- Siemens Healthcare Diagnostics, Inc.
- Product code
- Code MOI
- Advisory panel
- Immunology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Tarrytown, NY, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.