K251377
- 510(k) number
- K251377
- Device name
- Magic InBra
- Applicant
- Medela AG CH
- Product code
- HGX — Pump, Breast, Powered
- Decision date
- 2025-09-18
- Date received
- 2025-05-02
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Obstetrics/Gynecology
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K251377.pdf
Official FDA record: K251377
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.