BK231016 - Aeon ACKit
510(k) Number: BK231016
Applicant: Aeon Biotherapeutics Corp.
Device Name: Aeon ACKit
Decision Date: 02/16/2024
Supporting Documents
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: BK231016
Applicant: Aeon Biotherapeutics Corp.
Device Name: Aeon ACKit
Decision Date: 02/16/2024