# HHJ: Locator, Intracorporeal Device, Ultrasonic, Obstetric-Gynecologic

- Device class: 2; regulation: 21 CFR 884.2225; FDA's rule: 510(k) required
- FDA decisions: 1
- 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)
- 2002: 1

## Most-cited predicates
- K023227: USG 2000SA (2002), cited by 2

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