BK230806 - ImmuLINK (v3.0)
510(k) Number: BK230806
Applicant: Immucor, Inc.
Device Name: ImmuLINK (v3.0)
Decision Date: 4/25/2023
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: BK230806
Applicant: Immucor, Inc.
Device Name: ImmuLINK (v3.0)
Decision Date: 4/25/2023