Clearance Summary
LANSINOH POWERED ELECTRIC BREAST PUMP received FDA 510(k) clearance under submission number K122474, sponsored by Lansinoh Laboratories Saglik Gerecleri Tasarim San. 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 2012-12-28.
- Submission: K122474
- Applicant / Sponsor: Lansinoh Laboratories Saglik Gerecleri Tasarim San
- Clearance pathway: Special
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.5160
- Decision date: 2012-12-28
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.