# K072200: Stimlab

- Pathway: 510(k) (Traditional)
- Applicant: Micropace Pty, Ltd.
- Decided: Oct 26, 2007 after 79 days
- Product code: JOQ (Generator, Pulse, Pacemaker, External Programmable (For Electrophysiological Studies Only))
- Device class: 2
- Regulation: 21 CFR 870.1750
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K854196 (1986). 2 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K011826: EPS320 Cardiac Stimulator, Micropace Pty, Ltd. (2002) Summary page 1.

## Most influential descendants
- K173439: Bloom2 Programmable Electrophysiology Stimulator (2018), 0 descendants of its own

## Indications for use
The StimLab Cardiac stimulator is intended to be used for diagnostic electrical stimulation of the heart for the purpose of initiation and termination of tachyarrhythmias, refractory measurements and measurements of electrical conduction.

Source page: https://510kreport.com/device/K072200
Methodology: https://510kreport.com/methodology