BK241080 - ImmuLINK (v3.2)
510(k) Number: BK241080
Applicant: Immucor, Inc.
Device Name: ImmuLINK (v3.2)
Decision Date: 8/6/2024
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: BK241080
Applicant: Immucor, Inc.
Device Name: ImmuLINK (v3.2)
Decision Date: 8/6/2024