BK220717 - AuraGen 123 Suction Lipoplasty System (A123)
510(k) Number: BK220717
Applicant: AuraGen Aesthetics LLC
Device Name: AuraGen 123 Suction Lipoplasty System (A123)
Decision Date: 5/3/2019
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: BK220717
Applicant: AuraGen Aesthetics LLC
Device Name: AuraGen 123 Suction Lipoplasty System (A123)
Decision Date: 5/3/2019