Clearance Summary
Electric Breast Pump (HL-3058 II Pro) received FDA 510(k) clearance under submission number K254125, sponsored by Fimilla (Shanghai) Maternity & Baby Articles Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 2026-05-13.
- Submission: K254125
- Applicant / Sponsor: Fimilla (Shanghai) Maternity & Baby Articles Co., Ltd.
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.5160
- Decision date: 2026-05-13
Classification & Regulation
This clearance is catalogued under FDA product code HGX and 21 CFR 884.5160, within the Obstetrics/Gynecology review panel as a Class II device.