# EQL: Laryngostroboscope

- Device class: 1; regulation: 21 CFR 874.4750; FDA's rule: 510(k) exempt
- FDA decisions: 8
- 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)
- 1977: 1
- 1980: 1
- 1982: 1
- 1984: 1
- 1989: 1
- 1992: 2
- 1999: 1

## Most-cited predicates
- K984521: Riwo Drive System 2302 with Generator, Small Motor Handles, 8563.111, 8563.351 (1999), cited by 2

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