BK210620 - BloodRelay 1.1.0
510(k) Number: BK210620
Applicant: Alliance Technologies, LLC
Device Name: BloodRelay 1.1.0
Decision Date: 10/4/2021
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: BK210620
Applicant: Alliance Technologies, LLC
Device Name: BloodRelay 1.1.0
Decision Date: 10/4/2021