meddevicedb.com FDA Device Reference

Breast Pump

K150923 Class II Traditional
Decision Date
2015-11-06
Sponsor / Applicant
Guangzhou Jinxinbao Electronic Co., Ltd.

Technical Specification

510(k) Submission ID K150923
Product Code HGX
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.5160
Decision Date 2015-11-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Breast Pump received FDA 510(k) clearance under submission number K150923, sponsored by Guangzhou Jinxinbao Electronic 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 2015-11-06.

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.