K230570
- 510(k) number
- K230570
- Device name
- Willow Generation 3 Breast Pump
- Applicant
- Willow Innovations, Inc. CA · US
- Product code
- HGX — Pump, Breast, Powered
- Decision date
- 2023-10-16
- Date received
- 2023-03-01
- 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: K230570.pdf
Official FDA record: K230570
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.