Spacelabs Medical, Inc. - FDA 510(k) Cleared Devices
35
Total
34
Cleared
0
Denied
Spacelabs Medical, Inc. has 34 FDA 510(k) cleared cardiovascular devices. Based in Hamden, US.
Historical record: 34 cleared submissions from 1993 to 2012.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
35 devices
Cleared
Mar 29, 2012
SPACELABS HEALTHCARE QUBE COMPACT MONITOR (91390
Cardiovascular
29d
Cleared
Nov 02, 2011
SPACELABS HEALTHCARE XPREZZON BESIDE MONITOR(9913930)
Cardiovascular
28d
Cleared
Dec 07, 2010
SPACELABS MEDICAL PATIENT MONITORS
Cardiovascular
104d
Cleared
Nov 24, 2009
ELANCE VITAL SIGNS MONITOR AND ELANCE CENTRAL STATION
Cardiovascular
12d
Cleared
Aug 01, 2008
MODIFICATION TO MCARE 300 VITAL SIGNS MONITOR, MODEL 91220
Cardiovascular
14d
Cleared
Mar 15, 2007
SPACELABS MEDICAL FULL DISCLOSURE SYSTEM, MODEL 91810
Cardiovascular
118d
Cleared
Sep 29, 2006
MCARE 300 VITAL SIGNS MONITOR, MODEL 91220
Cardiovascular
67d
Cleared
Sep 19, 2006
SPACELABS MEDICAL CLINICAL EVENT INTERFACE, MODEL 91847
Cardiovascular
43d
Cleared
Jun 23, 2006
SPACELABS MEDICAL BISPECTRAL INDEX (BISX) ANALYSIS MODULE 91482 AND...
Neurology
81d
Cleared
Apr 19, 2006
SPACELABS MEDICAL MULTIGAS ANALYZER MODULE 91518 AND ACCESSORIES
Anesthesiology
117d
Cleared
May 03, 2005
SPACELABS MEDICAL MULTIPARAMETER MODULE 91496
Cardiovascular
54d
Cleared
Mar 04, 2005
SPACELABS MEDICAL MULTIPARAMETER MODULE 91496
Cardiovascular
37d