K253149
- 510(k) number
- K253149
- Device name
- Motion InBra (YM-8801) wearable breast pump
- Applicant
- Medela, LLC IL · US
- Product code
- HGX — Pump, Breast, Powered
- Decision date
- 2026-02-13
- Date received
- 2025-09-25
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Obstetrics/Gynecology
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K253149.pdf
Official FDA record: K253149
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.