# LCC: Applicator, Ocular Pressure

- Device class: 2; regulation: 21 CFR 886.4610; FDA's rule: 510(k) required
- FDA decisions: 6
- 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)
- 1979: 1
- 1982: 1
- 1984: 1
- 1985: 1
- 1995: 1
- 2012: 1

## Most-cited predicates
- K820526: Relief Valve-Honan Intraoc. Pressure (1982), cited by 1

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