FDA 510(k) Applications Submitted by Ed Horton

FDA 510(k) Number	Submission Date	Device Name	Applicant
K980210	01/21/1998	VARIOUS SURGICAL OR PATIENT DRAPES	GEL-LITE, L.L.C.
K220498	02/22/2022	NovoGen Wound Matrix	Novabone Products, 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