Ablacon, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ablacon, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Ablamap® System, Ablacath™ Mapping Catheter, Ablamap Software
3
Total
3
Cleared
0
Denied
Ablacon, Inc. has 3 FDA 510(k) cleared medical devices. Based in Denver, US.
Last cleared in 2023. Active since 2021. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Ablacon, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Honkanen Consulting, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Ablacon, Inc.
3 devices