Atheromed, Inc. is one of 5120 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Atheromed, Inc. - FDA 510(k) Cleared Devices
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.
Atheromed, Inc. — FDA 510(k) Products and Clearance History
2 devices
Cleared
Aug 22, 2014
1.8 MM PHOENIX ATHERECTOMY CATHETER, 2.2 MM PHOENIX ATHERECTOMY CATHETER,...
Cardiovascular
130d
Cleared
Jan 17, 2014
PHOENIX 5F TRACKING ATHERECTOMY CATHETER, PHOENIX 6F TRACKING ATHERECTOMY...
Cardiovascular
142d