BK220668 - VorFat System
510(k) Number: BK220668
Applicant: Alma Lasers, Inc.
Device Name: VorFat System
Decision Date: 6/12/2023
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: BK220668
Applicant: Alma Lasers, Inc.
Device Name: VorFat System
Decision Date: 6/12/2023