BK241095 - Healeon Float PRP devices (HFPRP15, HFPRP30, and HFPRP45)
510(k) Number: BK241095
Applicant: Bimini Health Tech
Device Name: Healeon Float PRP devices (HFPRP15, HFPRP30, and HFPRP45)
Decision Date: 11/20/2024
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: BK241095
Applicant: Bimini Health Tech
Device Name: Healeon Float PRP devices (HFPRP15, HFPRP30, and HFPRP45)
Decision Date: 11/20/2024