Cardiac Science Corporation is one of 18444 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cardiac Science Corporation - FDA 510(k) Cleared Devices
Recent clearances: Powerheart G5 AED, POWERHEART G5 AED, MYSENSE HEART
10
Total
10
Cleared
0
Denied
Cardiac Science Corporation has 10 FDA 510(k) cleared cardiovascular devices. Based in Bothell, US.
Historical record: 10 cleared submissions from 2006 to 2015.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Cardiac Science Corporation
10 devices
Cleared
May 04, 2015
Powerheart G5 AED
Cardiovascular
126d
Cleared
Feb 12, 2014
POWERHEART G5 AED
Cardiovascular
520d
Cleared
CT
Dec 21, 2011
MYSENSE HEART
Cardiovascular
54d
Cleared
Jun 09, 2011
POWERHEART AED G3 SEMI-AUTOMATIC, POWERHEART AED G3 AUTOMATIC, POWERHEART AED...
Cardiovascular
282d
Cleared
Jun 03, 2010
CARECENTER MD
Cardiovascular
233d
Cleared
Sep 10, 2009
POWERHEART AED G3, MODEL 9390E, POWERHEART AED G3 AUTOMATIC, MODEL 9390A
Cardiovascular
72d
Cleared
Dec 12, 2008
9131 DEFIBRILLATION ELECTRODES
Cardiovascular
141d
Cleared
Aug 26, 2008
Q-STRESS AND HEARTSTRIDE, MODELS QSTRESS/Q40 AND H4/H4S
Cardiovascular
25d
Cleared
May 15, 2006
MODIFICATION TO POWERHEART ECD
Cardiovascular
40d
Cleared
Apr 19, 2006
ATRIA 3100, ATRIA 6100
Cardiovascular
86d