BK200471 - Reapplix 3C Patch System
510(k) Number: BK200471
Applicant: Reapplix A/S
Device Name: Reapplix 3C Patch System
Decision Date: 1/13/2021
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: BK200471
Applicant: Reapplix A/S
Device Name: Reapplix 3C Patch System
Decision Date: 1/13/2021