Clearance Summary
Motion InBra (YM-8801) wearable breast pump received FDA 510(k) clearance under submission number K253149, sponsored by Medela, LLC. 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 2026-02-13.
- Submission: K253149
- Applicant / Sponsor: Medela, LLC
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.5160
- Decision date: 2026-02-13
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.