Dako Denmark A/S is one of 94 FDA 510(k) medical device manufacturers from Denmark in the dataset, ranked by real submission volume.
Dako Denmark A/S - FDA 510(k) Cleared Devices
Recent clearances: FLEX Monoclonal Mouse Anti-Human Progesterone Receptor, Clone PgR 1294, Ready-to-Use (Dako Omnis), FLEX Monoclonal Rabbit Anti-Human Estrogen Receptor a, Clone EPI, RTU (Dako Onmis)
2
Total
2
Cleared
0
Denied
Dako Denmark A/S has 2 FDA 510(k) cleared medical devices. Based in Golstrup, DK.
Historical record: 2 cleared submissions from 2017 to 2017. Primary specialty: Pathology.
Browse the FDA 510(k) cleared devices submitted by Dako Denmark A/S Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Dako Denmark A/S
2 devices