BK210653 - ORTHO Daily QC Simulated Whole Blood Quality Control Kit
510(k) Number: BK210653
Applicant: Millipore (UK) Ltd.
Device Name: ORTHO™ Daily QC Simulated Whole Blood Quality Control Kit
Decision Date: 6/7/2022
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: BK210653
Applicant: Millipore (UK) Ltd.
Device Name: ORTHO™ Daily QC Simulated Whole Blood Quality Control Kit
Decision Date: 6/7/2022