Ichor Vascular, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ichor Vascular, Inc. - FDA 510(k) Cleared Devices
Recent clearances: The ICHOR Panacea Vascular Embolectomy Catheter System
1
Total
1
Cleared
0
Denied
Ichor Vascular, Inc. has 1 FDA 510(k) cleared medical devices. Based in Toledo, US.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Ichor Vascular, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Namsa as regulatory consultant.
FDA 510(k) Regulatory Record - Ichor Vascular, Inc.
1 devices