Clearance Summary
HANDHELD MANUAL BREAST PUMP (AVENT MANUAL BREAST PUMP) received FDA 510(k) clearance under submission number K101538, sponsored by Philips Electronics UK Limited. 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 2010-11-05.
- Submission: K101538
- Applicant / Sponsor: Philips Electronics UK Limited
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class I
- Regulation citation: 21 CFR 884.5150
- Decision date: 2010-11-05
Classification & Regulation
This clearance is catalogued under FDA product code HGY and 21 CFR 884.5150, within the Obstetrics/Gynecology review panel as a Class I device.