BK231039 - Giotto Monza (BCS03)
510(k) Number: BK231039
Applicant: Delcon S.r.l.
Device Name: Giotto Monza (BCS03)
Decision Date: 3/26/2025
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: BK231039
Applicant: Delcon S.r.l.
Device Name: Giotto Monza (BCS03)
Decision Date: 3/26/2025