BK220714 - LipiVage
510(k) Number: BK220714
Applicant: Genesis Biosystems Inc.
Device Name: LipiVage
Decision Date: 12/8/2017
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: BK220714
Applicant: Genesis Biosystems Inc.
Device Name: LipiVage
Decision Date: 12/8/2017