BK210564 - ORTHO VISION Max Analyzer
510(k) Number: BK210564
Applicant: Ortho-Clinical Diagnostics, Inc.
Device Name: ORTHO VISION® Max Analyzer
Decision Date: 5/13/2021
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: BK210564
Applicant: Ortho-Clinical Diagnostics, Inc.
Device Name: ORTHO VISION® Max Analyzer
Decision Date: 5/13/2021