Agendia, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Agendia, Inc. - FDA 510(k) Cleared Devices
Recent clearances: MammaPrint FFPE NGS Kit, MammaPrint
2
Total
2
Cleared
0
Denied
Agendia, Inc. has 2 FDA 510(k) cleared medical devices. Based in Irvina, US.
Last cleared in 2022. Active since 2020. Primary specialty: Pathology.
Browse the FDA 510(k) cleared devices submitted by Agendia, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant.
FDA 510(k) Regulatory Record - Agendia, Inc.
2 devices