Diagenode is one of 33 FDA 510(k) medical device manufacturers from Belgium in the dataset, ranked by real submission volume.
Diagenode - FDA 510(k) Cleared Devices
Recent clearances: Panther Fusion GBS Assay
1
Total
1
Cleared
0
Denied
Diagenode has 1 FDA 510(k) cleared medical devices. Based in Seraing, BE.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Diagenode Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Axteria Biomed Consulting, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Diagenode
1 devices