HHK
- Product code
- HHK
- Device name
- Curette, Suction, Endometrial (And Accessories)
- Device class
- Class 2
- 21 CFR
- 21 CFR 884.1175
- Medical specialty
- Obstetrics/Gynecology
- Marketing pathway
- 510(K)
- Flag
- Third-party review eligible
- 510(k) clearances (last 3 years)
- 2
- Summaries archived here
- 1 (direct download)
- 510(k) clearances (all years, FDA)
- 42 (all years; only the last 3 years are listed here)
510(k) clearances, last 3 years (2)
| Number | Decision date | Applicant | Device name | Summary |
|---|---|---|---|---|
| K251882 | 2025-10-16 | Gcmedica Enterprise Ltd.(Wuxi) | Uterine Aspiration Set | |
| K240434 | 2024-09-25 | Li Medical Corporation , Ltd. | RELIEEV Suction Curette (Flexible 3.0/ Standard 3.6) | FDA |
Official FDA classification page: HHK
Classification and pathway per current FDA publications. Data from openFDA (CC0).