FDA 510(k) Applications for Medical Device Product Code: JOQ (Generator, Pulse, Pacemaker, External Programmable)

FDA 510(k) Applications for Medical Device Product Code "JOQ"
(Generator, Pulse, Pacemaker, External Programmable)

FDA 510(k) Number	Applicant	Device Name	Decision Date
K040207	EP MEDSYSTEMS	EP-4 CLINICAL STIMULATOR	02/27/2004
K041442	EP MEDSYSTEMS	EP-4 CLINICAL STIMUTATOR	09/14/2004
K092913	EP MEDSYSTEMS	EP-4TM CARDIAC STIMULATOR, MODELS: EP-04-02, EP-04-04	10/16/2009
K173439	Fischer Medical	Bloom2 Programmable Electrophysiology Stimulator	03/29/2018
K991293	FISCHER MEDICAL TECHNOLOGIES, INC.	EPSTIM ELECTROPHYSIOLOGY STIMULATOR CONTROL PROGRAM, BLOOM DTU-215 ELECTROPHYSIOLOGY PROGRAMMABLE STIMULATOR	05/05/2000
K011826	MICROPACE PTY. LTD.	EPS320 CARDIAC STIMULATOR	01/24/2002
K072200	MICROPACE PTY. LTD.	STIMLAB	10/26/2007
K963579	RADIONICS, INC.	PACE-1A CARDIAC STIMULATOR	11/08/1996
K070743	ST CARDIO TECHNOLOGIES, LLC	Z6 STIMULATOR	07/02/2007