Inovise Medical, Inc. - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
Inovise Medical, Inc. has 14 FDA 510(k) cleared cardiovascular devices. Based in Newberg, US.
Historical record: 14 cleared submissions from 2000 to 2016.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
14 devices
Cleared
Mar 18, 2016
AUDICOR CA300/CC100 Analyzer with SDB
Anesthesiology
295d
Cleared
Apr 11, 2014
AUDICOR CPAM WITH SDB (ACCELEROMETER BASED)
Anesthesiology
290d
Cleared
Oct 11, 2013
AUDICOR CPAM WITH SDB (SINGLE SENSOR)
Cardiovascular
213d
Cleared
Sep 20, 2012
AUDICOR CPAM WITH SDB (CARDIOPULMONARY AMBULATORY MONITOR WITH SLEEP...
Cardiovascular
218d
Cleared
Oct 24, 2011
AUDICOR CPAM (CARDIOPULMONARY AMBULATORY MONITOR)
Cardiovascular
238d
Cleared
Feb 04, 2011
AUDICOR SENSOR-ADAPTER MODEL AUDICOR SENSOR-ADAPTER 4.0
Cardiovascular
66d
Cleared
Sep 25, 2008
AUDICOR SENSOR, MODELS: 2.0, 3.0
Cardiovascular
206d
Cleared
Sep 09, 2008
AUDICOR, HEMO AMBULATORY MONITOR
Cardiovascular
266d
Cleared
Apr 13, 2007
AUDICOR 200 SYSTEM, MODELS 200D AND 200S
Cardiovascular
87d
Cleared
Nov 10, 2005
EXTENDED MEASUREMENTS SYSTEM
Cardiovascular
161d
Cleared
Feb 22, 2005
LIBERTY SYSTEM
Cardiovascular
106d
Cleared
Oct 31, 2003
AUDICOR UPGRADE SYSTEM
Cardiovascular
109d
Cleared
Aug 07, 2003
AUDICOR COR SENSOR (AND ACCESSORY ADAPTOR)
Cardiovascular
189d
Cleared
Jul 27, 2000
CARDIOVISE ECG INTERPRETATIVE SOFTWARE
Cardiovascular
90d