BK210591 - Platelet-Rich Plasma (PRP) Procedure Pack
510(k) Number: BK210591
Applicant: Terumo BCT, Inc
Device Name: Platelet-Rich Plasma (PRP) Procedure Pack
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: BK210591
Applicant: Terumo BCT, Inc
Device Name: Platelet-Rich Plasma (PRP) Procedure Pack
Decision Date: 2/11/2022