Atlas FDA

Lifeline/ReviveR DDU-100, Lifeline/ReviveR AUTO DDU-120, Lifeline/ReviveR VIEW DDU-2300, Lifeline/ReviveR VIEW AUTO DDU-

FDA premarket approval P160032 · decided 2018-02-01

Approval details

PMA number
P160032
Trade name
Lifeline/ReviveR DDU-100, Lifeline/ReviveR AUTO DDU-120, Lifeline/ReviveR VIEW DDU-2300, Lifeline/ReviveR VIEW AUTO DDU-
Generic name
Automated external defibrillators (non-wearable)
Applicant
Defibtech, LLC
Date received
2016-08-02
Decision date
2018-02-01
Days to decision
548 days
Decision code
APPR
Product code
MKJ
Advisory committee
Cardiovascular
Expedited review
No
Location
Guilford, CT
Statement
Approval of the Lifeline/ReviveR DDU-100, Lifeline/ReviveR AUTO DDU-120, Lifeline/ReviveR VIEW DDU-2300, Lifeline/ReviveR VIEW AUTO DDU-2200, Lifeline/ReviveR ECG DDU-2450, and Lifeline/ReviveR ECG+ DDU-2475 Automated External Defibrillators.The Lifeline/ReviveR DDU-100 series Automated External Defibrillator (AED) is indicated for use on victims of sudden cardiac arrest (SCA) who are:1) Unconscious and unresponsive; and2) Not breathing or not breathing normally.Lifeline/ReviveR DDU-100 series A

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510(k) clearances by this applicant

RecordFirmDate
RMU-2000 Automated Chest Compression System (K211289)Defibtech, LLC2021-11-09
RMU-1000 AUTOMATED CHEST COMPRESSION SYSTEM (K141809)Defibtech, LLC2014-10-27
SEMIAUTOMATIC EXTERNAL DEFIBRILLATOR AND ACCESSORIES (K131525)Defibtech, LLC2014-04-24
DDU-120 FULLY AUTOMATIC EXTERNAL DEFIBRILLATOR AND ACCESSORIES (K113787)Defibtech, LLC2013-01-04
DDU-2400/2450 SEMIAUTOMATIC EXTERNAL DEFIBRILLATOR AND ACCESSORIES (K121853)Defibtech, LLC2012-12-13
DDU-2300 SEMIAUTOMATIC EXTERNAL DEFIBRILLATOR AND ACCESSORIES (K081259)Defibtech, LLC2009-06-15
DEFIBTECH AED WITH ATTENUATED DEFIBRILLATION/MONITORING PADS, MODELS DDU-100 WITH DDP-200P (K033896)Defibtech, LLC2004-06-16
DEFIBTECH ELECTRODE ADAPTER, MODEL DAC-300 SERIES (K033144)Defibtech, LLC2003-11-13