Hotspur Technologies is one of 5196 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Hotspur Technologies - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Hotspur Technologies has 5 FDA 510(k) cleared medical devices. Based in Mountain View, US.
Historical record: 5 cleared submissions from 2010 to 2013. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Hotspur Technologies Filter by specialty or product code using the sidebar.
Hotspur Technologies — FDA 510(k) Products and Clearance History
5 devices
Cleared
Jun 20, 2013
ARROW GPSCATH BALLOON DILATATION CATHETER
Cardiovascular
121d
Cleared
Jan 20, 2012
GPSCATH BALLON DILATATION CATHETER
Cardiovascular
29d
Cleared
Jul 13, 2010
PTA-DUO PTA BALLOON CATHETER
Cardiovascular
90d
Cleared
Jul 12, 2010
EMBO PLUS EMBOLECTOMY CATHETER
Cardiovascular
110d
Cleared
Jul 12, 2010
PTA-PLUS PTA BALLOON CATHER 5 MM X 4CM, PTA-PLUS PTA BALLOON CATHETER 6MM X 4CM
Cardiovascular
109d