BK220724 - ORTHO Optix Reader
510(k) Number: BK220724
Applicant: Ortho-Clinical Diagnostics, Inc.
Device Name: ORTHO Optix™ Reader
Decision Date: 6/24/2022
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: BK220724
Applicant: Ortho-Clinical Diagnostics, Inc.
Device Name: ORTHO Optix™ Reader
Decision Date: 6/24/2022