Clearance Summary
Momcozy Wearable Electric Breast Pump ( Model: S9 Pro, S12 Pro) received FDA 510(k) clearance under submission number K230776, sponsored by Shenzhen Lutejiacheng Technology 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 2023-06-09.
- Submission: K230776
- Applicant / Sponsor: Shenzhen Lutejiacheng Technology Co., Ltd.
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.5160
- Decision date: 2023-06-09
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.