HHJ
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Locator, Intracorporeal Device, Ultrasonic, Obstetric-Gynecologic
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 884.2225
- Medical specialty
- Obstetrics/Gynecology
- Flags
- Third-party review eligible
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| USG 2000SA (K023227) | Ultraguide , Ltd. | 2002-10-22 |
Track HHJ automatically
Every clearance here is in the API, with alerts when new ones post.