meddevicedb.com FDA Device Reference

Electric Breast Pump

K191802 Class II Traditional
Decision Date
2020-01-16
Sponsor / Applicant
Ningbo Huiyoo Baby Products Co., Ltd.

Technical Specification

510(k) Submission ID K191802
Product Code HGX
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.5160
Decision Date 2020-01-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Electric Breast Pump received FDA 510(k) clearance under submission number K191802, sponsored by Ningbo Huiyoo Baby Products 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 2020-01-16.

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.