FDA 510(k) Applications Submitted by CARDIAC SCIENCE, INC.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K022210 |
07/08/2002 |
MULTIFUNCTIONAL ELECTRODE MODELS 9640, 9650 |
CARDIAC SCIENCE, INC. |
K022929 |
09/04/2002 |
PEDIATRIC ATTENUATED DEFIBRILLATION ELECTRODES, MODEL 9730, POWEDERHEART AED, MODEL 9200/9210 |
CARDIAC SCIENCE, INC. |
K040438 |
02/19/2004 |
POWERHEART AED G3A |
CARDIAC SCIENCE, INC. |
K040637 |
03/10/2004 |
POWERHEART AED G3 PRO |
CARDIAC SCIENCE, INC. |
K052316 |
08/25/2005 |
POWERHEART ECD |
CARDIAC SCIENCE, INC. |
K052161 |
08/09/2005 |
POWERHEART AED G3 (MODEL 9390E), POWERHEART AED G3 AUTOMATIC (MODEL 9390A) |
CARDIAC SCIENCE, INC. |
K970741 |
02/28/1997 |
POWERHEART AECD |
CARDIAC SCIENCE, INC. |
K012197 |
07/13/2001 |
POWERHEART CARDIAC RHYTHM MODULE |
CARDIAC SCIENCE, INC. |
K982710 |
08/04/1998 |
AECD ARRHYTHMIA DETECTION SOFTWARE |
CARDIAC SCIENCE, INC. |
K993533 |
10/19/1999 |
POWERHEART AECD |
CARDIAC SCIENCE, INC. |
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