meddevicedb.com FDA Device Reference

Electric breast pump (Models: RH-228 and RH-338)

K201903 Class II Traditional
Decision Date
2021-04-09
Sponsor / Applicant
Cixi Ruihong Electric Appliance Co., Ltd.

Technical Specification

510(k) Submission ID K201903
Product Code HGX
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.5160
Decision Date 2021-04-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Electric breast pump (Models: RH-228 and RH-338) received FDA 510(k) clearance under submission number K201903, sponsored by Cixi Ruihong Electric Appliance 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 2021-04-09.

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.