# JOQ: Generator, Pulse, Pacemaker, External Programmable (For Electrophysiological Studies Only)

- Device class: 2; regulation: 21 CFR 870.1750; FDA's rule: 510(k) required
- FDA decisions: 19
- Recalls: 3 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026; MAUDE to Sep 30, 2026

## Decisions per year (last 10)
- 1994: 2
- 1995: 1
- 1996: 3
- 1998: 1
- 2000: 2
- 2002: 1
- 2004: 2
- 2007: 2
- 2009: 1
- 2018: 1

## Most-cited predicates
- K011826: EPS320 Cardiac Stimulator (2002), cited by 4
- K072200: Stimlab (2007), cited by 1
- K991293: Epstim Electrophysiology Stimulator Control Program, Bloom Dtu-215 Electrophysiology Programmable Stimulator (2000), cited by 1
- K040207: EP-4 Clinical Stimulator (2004), cited by 1

Source page: https://510kreport.com/product-code/JOQ
Data by year (CSV): https://510kreport.com/product-code/JOQ.csv