Ichor is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ichor - FDA 510(k) Cleared Devices
Recent clearances: ICHOR 7F Embolectomy System (ICH-7F), ICHOR 14F Embolectomy System
2
Total
2
Cleared
0
Denied
Ichor has 2 FDA 510(k) cleared medical devices. Based in Boca Raton, US.
Latest FDA clearance: Jul 2024. Active since 2023. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Ichor Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ichor
2 devices