Cardiac Science Corporation
FDA 510(k) & PMA Approved Devices — 8 products
Advertisement
Total Devices8
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K113176 | MYSENSE HEART | DSH | 2011-12-21 | View |
| 510(k) | K102496 | POWERHEART AED G3 SEMI-AUTOMATIC, POWERHEART AED G3 AUTOMATIC, POWERHEART AED G3 PRO, POWERHEART AED G3 PLUS | MKJ | 2011-06-09 | View |
| 510(k) | K093211 | CARECENTER MD | DPS | 2010-06-03 | View |
| 510(k) | K091943 | POWERHEART AED G3, MODEL 9390E, POWERHEART AED G3 AUTOMATIC, MODEL 9390A | MKJ | 2009-09-10 | View |
| 510(k) | K082090 | 9131 DEFIBRILLATION ELECTRODES | MKJ | 2008-12-12 | View |
| 510(k) | K082173 | Q-STRESS AND HEARTSTRIDE, MODELS QSTRESS/Q40 AND H4/H4S | DPS | 2008-08-26 | View |
| 510(k) | K060934 | MODIFICATION TO POWERHEART ECD | MKJ | 2006-05-15 | View |
| 510(k) | K060167 | ATRIA 3100, ATRIA 6100 | DPS | 2006-04-19 | View |
No matching devices.
Advertisement