Micrus Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Micrus Corp. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Micrus Corp. has 6 FDA 510(k) cleared medical devices. Based in Mountain View, US.
Historical record: 6 cleared submissions from 2001 to 2004. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Micrus Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Micrus Corp.
6 devices
Cleared
Feb 04, 2004
MICRUS MODIFIED MICROCOIL SYSTEM, CERECYTE
Neurology
57d
Cleared
Nov 28, 2003
MICRUS MICROCOIL SYSTEM
Neurology
74d
Cleared
Sep 10, 2003
MICRUS MICROCATHETER
Cardiovascular
15d
Cleared
Aug 01, 2003
MICRUS MICROCOIL SYSTEMS, MODELS HEL, SPH, STR, FSR AND HSR
Neurology
73d
Cleared
Oct 22, 2002
MICRUS STRETCH-RESISTANT MICROCOIL SYSTEM, MSR01
Neurology
90d
Cleared
Jan 11, 2001
MICRUS MICROCOIL DELIVERY SYSTEM, MDS03
Neurology
189d