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Wearable Breast Pump (P9, P10, P16, P20, P21, P22, P23, P25)

K252192 Class II Special
Decision Date
2025-08-13
Sponsor / Applicant
Huizhou Lvb Maternal and Infant Supplies Co., Ltd.

Technical Specification

510(k) Submission ID K252192
Product Code HGX
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.5160
Decision Date 2025-08-13
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Wearable Breast Pump (P9, P10, P16, P20, P21, P22, P23, P25) received FDA 510(k) clearance under submission number K252192, sponsored by Huizhou Lvb Maternal and Infant Supplies Co., Ltd.. The device was reviewed via the Special premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 2025-08-13.

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.