BK220674 - MicroAire LipoFilter System
510(k) Number: BK220674
Applicant: MicroAire Surgical Instruments, LLC.
Device Name: MicroAire LipoFilter® System
Decision Date: 3/16/2022
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: BK220674
Applicant: MicroAire Surgical Instruments, LLC.
Device Name: MicroAire LipoFilter® System
Decision Date: 3/16/2022