Defibtech, LLC
FDA 510(k) & PMA Approved Devices — 7 products
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Total Devices7
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K211289 | RMU-2000 Automated Chest Compression System | DRM | 2021-11-09 | View |
| 510(k) | K113787 | DDU-120 FULLY AUTOMATIC EXTERNAL DEFIBRILLATOR AND ACCESSORIES | MKJ | 2013-01-04 | View |
| 510(k) | K121853 | DDU-2400/2450 SEMIAUTOMATIC EXTERNAL DEFIBRILLATOR AND ACCESSORIES | MKJ | 2012-12-13 | View |
| 510(k) | K081259 | DDU-2300 SEMIAUTOMATIC EXTERNAL DEFIBRILLATOR AND ACCESSORIES | MKJ | 2009-06-15 | View |
| 510(k) | K033896 | DEFIBTECH AED WITH ATTENUATED DEFIBRILLATION/MONITORING PADS, MODELS DDU-100 WITH DDP-200P | MKJ | 2004-06-16 | View |
| 510(k) | K033144 | DEFIBTECH ELECTRODE ADAPTER, MODEL DAC-300 SERIES | MKJ | 2003-11-13 | View |
| 510(k) | K013896 | SENTRY SEMIAUTOMATIC EXTERNAL DEFIBRILLATOR; EXTERNAL DEFIBRILLATION PADS (ELECTRODES) DDP-100; BATTERY PACK 1200MAH; BA | MKJ | 2002-06-19 | View |
No matching devices.
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