Micrus Endovascular Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Micrus Endovascular Corporation - FDA 510(k) Cleared Devices
23
Total
23
Cleared
0
Denied
Micrus Endovascular Corporation has 23 FDA 510(k) cleared medical devices. Based in Sunnyvale, US.
Historical record: 23 cleared submissions from 2005 to 2011. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Micrus Endovascular Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Micrus Endovascular Corporation
23 devices
Cleared
Jan 26, 2011
MICRUS ASCENT OCCLUSION BALLOON CATHETER 4X7 MM
Cardiovascular
30d
Cleared
Dec 03, 2010
MICRUS ONE 2 ONE GUIDEWIRE, MICRUS ONE 2 ONE SOFT GUIDEWIRE
Cardiovascular
66d
Cleared
Nov 20, 2009
MICRUS MICROCATHETER, MODEL COURIER 270
Cardiovascular
79d
Cleared
Jun 19, 2009
MICRUS ASCENT OCCLUSION BALLOON CATHETER 4X7MM,6X9MM, MICRUS SUMMIT OCCLUSION...
Cardiovascular
29d
Cleared
May 06, 2009
MICRUS MICROCATHETER, COURIER FLEX, MODEL MSF 170000-00
Cardiovascular
126d
Cleared
Mar 03, 2009
MICRUS ONE 2 ONE GUIDEWIRE AND SOFT GUIDEWIRE
Cardiovascular
27d
Cleared
Jan 02, 2009
MICRUS MICROCOLI SYSTEM, DELTAPLUSH, MODELS CPL, DPL
Neurology
24d
Cleared
Oct 17, 2008
MICRUS MICROCOIL DELIVERY SYSTEM
Neurology
29d
Cleared
Aug 27, 2008
MICRUS ASCENT OCCLUSION BALLOON CATHETER
Cardiovascular
153d
Cleared
Jun 30, 2008
MICRUS MICROCOIL SYSTEM, DELTAPAQ 10 STRETCH RESISTANT
Neurology
138d
Cleared
May 08, 2008
MICRUS MICROCOIL SYSTEM, DELTAPAQ 10 CERECYTE, MODEL CDF
Neurology
83d
Cleared
Feb 26, 2008
MICRUS MICROCOIL SYSTEMS
Neurology
81d