BK210608 - Galileo Echo
510(k) Number: BK210608
Applicant: Immucor, Inc.
Device Name: Galileo Echo
Decision Date: 1/8/2025
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: BK210608
Applicant: Immucor, Inc.
Device Name: Galileo Echo
Decision Date: 1/8/2025