JOQ · Class II · 21 CFR 870.1750

FDA Product Code JOQ: Generator, Pulse, Pacemaker, External Programmable (for Electrophysiological Studies Only)

Leading manufacturers include Medtronic Vascular, Fischer Medical and Cordis Corp..

18
Total
18
Cleared
114d
Avg days
1984
Since

FDA 510(k) Cleared Generator, Pulse, Pacemaker, External Programmable (for Electrophysiological Studies Only) Devices (Product Code JOQ)

18 devices
1–18 of 18
Cleared Mar 29, 2018
Bloom2 Programmable Electrophysiology Stimulator
K173439
Fischer Medical
Cardiovascular · 146d
Cleared Aug 04, 1986
MEDTRONIC MODEL 5328 PROGRAMMABLE STIMULATOR
K861368
Medtronic Vascular
Cardiovascular · 115d
Cleared Jun 11, 1985
CORDIS ELECTROPHYSIOLOGY STIMULATOR
K844815
Cordis Corp.
Cardiovascular · 182d
Cleared Apr 16, 1985
MEDTRONIC MODEL 5328 PROGRAM-STIMULATOR
K851091
Medtronic Vascular
Cardiovascular · 29d
Cleared Sep 27, 1984
PROGRAMMABLE STIMULATOR 5326
K843718
Medtronic Vascular
Cardiovascular · 3d
Cleared Jan 30, 1984
PROGRAMMABLE STIMULATOR 2352
K833421
Medtronic Vascular
Cardiovascular · 119d

About Product Code JOQ - Regulatory Context