# KCX: Epilator, High Frequency, Tweezer-Type

- Device class: 1; regulation: 21 CFR 878.5360; FDA's rule: 510(k) exempt
- FDA decisions: 25
- 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
- 1980: 1
- 1981: 1
- 1984: 2
- 1985: 1
- 1990: 1
- 1991: 1
- 1992: 1
- 1995: 2
- 1997: 7

## Most-cited predicates
- K892514: Ahrs Epilator 629 (1990), cited by 2
- K952117: Epilator (1995), cited by 1

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