BK220763 - LIFECODES LifeScreen XP
510(k) Number: BK220763
Applicant: Immucor GTI Diagnostics, Inc.
Device Name: LIFECODES LifeScreen XP
Decision Date: 9/29/2022
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: BK220763
Applicant: Immucor GTI Diagnostics, Inc.
Device Name: LIFECODES LifeScreen XP
Decision Date: 9/29/2022