Atheromed, Inc. is one of 19258 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Atheromed, Inc. - FDA 510(k) Cleared Devices
Recent clearances: 1.8 MM PHOENIX ATHERECTOMY CATHETER, 2.2 MM PHOENIX ATHERECTOMY CATHETER, PHOENIX HANDLE, PHOENIX WIRE SUPPORT CLIP, PHOENIX 5F TRACKING ATHERECTOMY CATHETER, PHOENIX 6F TRACKING ATHERECTOMY CATHETER, PHOENIX 7D DEFLECTING ATHERECTOMY CA
2
Total
2
Cleared
0
Denied
Atheromed, Inc. has 2 FDA 510(k) cleared medical devices. Based in Menlo Park, US.
Historical record: 2 cleared submissions from 2014 to 2014. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Atheromed, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Atheromed, Inc.
2 devices