K251882 is an FDA 510(k) clearance for the Uterine Aspiration Set. This device is classified as a Curette, Suction, Endometrial (and Accessories) (Class II - Special Controls, product code HHK).
Submitted by Gcmedica Enterprise Ltd.(Wuxi) (Wuxi, CN). The FDA issued a Cleared decision on October 16, 2025, 118 days after receiving the submission on June 20, 2025.
This device falls under the Obstetrics & Gynecology FDA review panel. Regulated under 21 CFR 884.1175.
| 510(k) Number | K251882 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | June 20, 2025 |
| Decision Date | October 16, 2025 |
| Days to Decision | 118 days |
| Submission Type | Traditional |
| Review Panel | Obstetrics & Gynecology (OB) |
| Summary | Summary PDF |
| Product Code | HHK - Curette, Suction, Endometrial (and Accessories) |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 884.1175 |