Somanetics Corp. is one of 20558 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Somanetics Corp. - FDA 510(k) Cleared Devices
Recent clearances: VITAL SYNC MODEL 5000 SERIES, OXYALERT NIRSENSORS, ACCESSORIES FOR INVOS 5100C SYSTEM, MODELS: IS-C AND IS-S, INVOS CEREBRAL/SOMATIC OXIMETER SYSTEM, MODEL: 5100C
12
Total
12
Cleared
0
Denied
Somanetics Corp. has 12 FDA 510(k) cleared medical devices. Based in Troy, US.
Historical record: 12 cleared submissions from 1990 to 2010. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Somanetics Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Somanetics Corp.
12 devices
Cleared
Apr 29, 2010
VITAL SYNC MODEL 5000 SERIES
Cardiovascular
177d
Cleared
Jul 09, 2009
OXYALERT NIRSENSORS, ACCESSORIES FOR INVOS 5100C SYSTEM, MODELS: IS-C AND IS-S
Cardiovascular
73d
Cleared
Apr 03, 2009
INVOS CEREBRAL/SOMATIC OXIMETER SYSTEM, MODEL: 5100C
Cardiovascular
232d
Cleared
May 14, 2008
INVOS CEREBRAL/SOMATIC OXIMETER SYSTEM, MODEL 5100C
Cardiovascular
57d
Cleared
Nov 04, 2005
INVOS SYSTEM
Cardiovascular
171d
Cleared
Mar 16, 2004
CORRESTORE PATCH SYSTEM
Cardiovascular
50d
Cleared
Aug 07, 2003
CORRESTORE PATCH SYSTEM
Cardiovascular
78d
Cleared
Nov 21, 2001
CORRESTORE PATCH, MODELS 1.5P2, 2P3, 3P4
Cardiovascular
190d
Cleared
Sep 15, 2000
ADULT/PEDIATRIC CEREBRAL OXIMETER, MODEL INVOS 5100
Anesthesiology
88d
Cleared
Oct 10, 1997
SOMANETICS INVOS 3100A CEREBRAL OXIMETER (INVOS)
Anesthesiology
161d
Cleared
Jun 05, 1996
SOMANETICS INVOS 3100A CEREBRAL OXIMETER (INVOS)
Anesthesiology
113d
Cleared
May 18, 1990
CAV SAT OXIMETER MODEL 100
Anesthesiology
410d