BK241067 – MatchX
510(k) Number: BK241067
Applicant: Immucor GTI Diagnostics, Inc.
Device Name: MatchX
Decision Date: 1/2/2025
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: BK241067
Applicant: Immucor GTI Diagnostics, Inc.
Device Name: MatchX
Decision Date: 1/2/2025