BK210632 - Royal MAXX PRP Concentration System
510(k) Number: BK210632
Applicant: Royal Biologics, Inc.
Device Name: Royal MAXX PRP Concentration System
Decision Date: 2/11/2022
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: BK210632
Applicant: Royal Biologics, Inc.
Device Name: Royal MAXX PRP Concentration System
Decision Date: 2/11/2022