# PIC: Oral Electronic Vision Aid

- Device class: 2; regulation: 21 CFR 886.5905; FDA's rule: 510(k) required
- FDA decisions: 2
- Recalls: 1 (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)
- 2015: 2

## Most-cited predicates
- DEN130039: Brainport V100 Device (2015), cited by 1

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