BK210563 - Royal Maxx Autologous PRP Concentration System
510(k) Number: BK210563
Applicant: Royal Biologics, Inc
Device Name: Royal Maxx Autologous PRP Concentration System
Decision Date: 4/16/2021
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: BK210563
Applicant: Royal Biologics, Inc
Device Name: Royal Maxx Autologous PRP Concentration System
Decision Date: 4/16/2021