Clearance Summary
Proture Double Electric Breast Pump received FDA 510(k) clearance under submission number K162747, sponsored by Guangdong Horigen Mother & 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 2016-12-08.
- Submission: K162747
- Applicant / Sponsor: Guangdong Horigen Mother & Baby Products Co., Ltd.
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.5160
- Decision date: 2016-12-08
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.