BK210558 - World PRP
510(k) Number: BK210558
Applicant: LUVO Medical Technologies, Inc.
Device Name: World PRP
Decision Date: 7/23/2021
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: BK210558
Applicant: LUVO Medical Technologies, Inc.
Device Name: World PRP
Decision Date: 7/23/2021