Cardiac Science, Inc.
FDA 510(k) & PMA Approved Devices — 10 products
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Total Devices10
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K052316 | POWERHEART ECD | MKJ | 2006-01-03 | View |
| 510(k) | K052161 | POWERHEART AED G3 (MODEL 9390E), POWERHEART AED G3 AUTOMATIC (MODEL 9390A) | MKJ | 2005-10-21 | View |
| 510(k) | K040637 | POWERHEART AED G3 PRO | MKJ | 2004-08-06 | View |
| 510(k) | K040438 | POWERHEART AED G3A | MKJ | 2004-07-01 | View |
| 510(k) | K022929 | PEDIATRIC ATTENUATED DEFIBRILLATION ELECTRODES, MODEL 9730, POWEDERHEART AED, MODEL 9200/9210 | MKJ | 2003-01-27 | View |
| 510(k) | K022210 | MULTIFUNCTIONAL ELECTRODE MODELS 9640, 9650 | MKJ | 2002-10-04 | View |
| 510(k) | K012197 | POWERHEART CARDIAC RHYTHM MODULE | MKJ | 2001-11-16 | View |
| 510(k) | K993533 | POWERHEART AECD | MKJ | 2000-01-24 | View |
| 510(k) | K982710 | AECD ARRHYTHMIA DETECTION SOFTWARE | MKJ | 1998-08-10 | View |
| 510(k) | K970741 | POWERHEART AECD | MKJ | 1997-10-16 | View |
No matching devices.
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