# LOT: Pulse-Generator, Program Module

- Device class: 3; regulation: 21 CFR —; FDA's rule: PMA required
- FDA decisions: 0
- Recalls: 0 (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)
- 1990: 1
- 1995: 1
- 1997: 1
- 1999: 1
- 2001: 2
- 2002: 1
- 2004: 1

## Most-cited predicates

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