Byteflies NV is one of 33 FDA 510(k) medical device manufacturers from Belgium in the dataset, ranked by real submission volume.
Byteflies NV - FDA 510(k) Cleared Devices
Recent clearances: Byteflies Kit
1
Total
1
Cleared
0
Denied
Byteflies NV has 1 FDA 510(k) cleared medical devices. Based in Antwerp, BE.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Byteflies NV Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Medicsense USA as regulatory consultant.
FDA 510(k) Regulatory Record - Byteflies NV
1 devices