BK230818 - Dr. PRP
510(k) Number: BK230818
Applicant: YTS Global Inc.
Device Name: Dr. PRP
Decision Date: 5/31/2023
Supporting Documents
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: BK230818
Applicant: YTS Global Inc.
Device Name: Dr. PRP
Decision Date: 5/31/2023