FDA 510(k) Applications Submitted by DEFIBTECH, LLC
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K211289 |
04/28/2021 |
RMU-2000 Automated Chest Compression System |
Defibtech, LLC |
| K081259 |
05/02/2008 |
DDU-2300 SEMIAUTOMATIC EXTERNAL DEFIBRILLATOR AND ACCESSORIES |
DEFIBTECH, LLC |
| K131525 |
05/28/2013 |
SEMIAUTOMATIC EXTERNAL DEFIBRILLATOR AND ACCESSORIES |
DEFIBTECH, LLC |
| K121853 |
06/25/2012 |
DDU-2400/2450 SEMIAUTOMATIC EXTERNAL DEFIBRILLATOR AND ACCESSORIES |
DEFIBTECH, LLC |
| K141809 |
07/07/2014 |
RMU-1000 AUTOMATED CHEST COMPRESSION SYSTEM |
DEFIBTECH, LLC |
| K113787 |
12/22/2011 |
DDU-120 FULLY AUTOMATIC EXTERNAL DEFIBRILLATOR AND ACCESSORIES |
DEFIBTECH, LLC |
| K013896 |
11/23/2001 |
SENTRY SEMIAUTOMATIC EXTERNAL DEFIBRILLATOR; EXTERNAL DEFIBRILLATION PADS (ELECTRODES) DDP-100; BATTERY PACK 1200MAH; BA |
DEFIBTECH, LLC |
| K033144 |
09/30/2003 |
DEFIBTECH ELECTRODE ADAPTER, MODEL DAC-300 SERIES |
DEFIBTECH, LLC |
| K033896 |
12/16/2003 |
DEFIBTECH AED WITH ATTENUATED DEFIBRILLATION/MONITORING PADS, MODELS DDU-100 WITH DDP-200P |
DEFIBTECH, LLC |
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