BK220721 - REVOLVE ENVI 600 Advanced Adipose System
510(k) Number: BK220721
Applicant: LifeCell Corporation
Device Name: REVOLVE ENVI 600 Advanced Adipose System
Decision Date: 5/28/2020
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: BK220721
Applicant: LifeCell Corporation
Device Name: REVOLVE ENVI 600 Advanced Adipose System
Decision Date: 5/28/2020