# DYC: Vectorcardiograph

- Device class: 2; regulation: 21 CFR 870.2400; FDA's rule: 510(k) required
- FDA decisions: 4
- 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)
- 1981: 1
- 1983: 1
- 1990: 1
- 2003: 1

## Most-cited predicates
- K896396: Mida System, Models 1000/1100 (1990), cited by 2

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