Defibtech, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Defibtech, LLC - FDA 510(k) Cleared Devices
Recent clearances: RMU-2000 Automated Chest Compression System
9
Total
8
Cleared
0
Denied
Defibtech, LLC has 8 FDA 510(k) cleared medical devices. Based in Guilford, US.
Last cleared in 2021. Active since 2002. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Defibtech, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Defibtech, LLC
9 devices
Cleared
Nov 09, 2021
RMU-2000 Automated Chest Compression System
Cardiovascular
195d
Cleared
Oct 27, 2014
RMU-1000 AUTOMATED CHEST COMPRESSION SYSTEM
Cardiovascular
112d
Cleared
Apr 24, 2014
SEMIAUTOMATIC EXTERNAL DEFIBRILLATOR AND ACCESSORIES
Cardiovascular
331d
Cleared
Jan 04, 2013
DDU-120 FULLY AUTOMATIC EXTERNAL DEFIBRILLATOR AND ACCESSORIES
Cardiovascular
379d
Cleared
Dec 13, 2012
DDU-2400/2450 SEMIAUTOMATIC EXTERNAL DEFIBRILLATOR AND ACCESSORIES
Cardiovascular
171d
Cleared
Jun 15, 2009
DDU-2300 SEMIAUTOMATIC EXTERNAL DEFIBRILLATOR AND ACCESSORIES
Cardiovascular
409d
Cleared
Jun 16, 2004
DEFIBTECH AED WITH ATTENUATED DEFIBRILLATION/MONITORING PADS, MODELS DDU-100...
Cardiovascular
183d
Cleared
Nov 13, 2003
DEFIBTECH ELECTRODE ADAPTER, MODEL DAC-300 SERIES
Cardiovascular
44d
Cleared
Jun 19, 2002
SENTRY SEMIAUTOMATIC EXTERNAL DEFIBRILLATOR
Cardiovascular
208d