Accurkardia, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Accurkardia, Inc. - FDA 510(k) Cleared Devices
Recent clearances: AccurECG Analysis System (v2.0), AccurECG Analysis System
2
Total
2
Cleared
0
Denied
Accurkardia, Inc. has 2 FDA 510(k) cleared medical devices. Based in New York, US.
Latest FDA clearance: Dec 2025. Active since 2023. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Accurkardia, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Medtech Impact Partners and Hyman, Phelps & McNamara, P.C..
FDA 510(k) Regulatory Record - Accurkardia, Inc.
2 devices