K231785
- 510(k) number
- K231785
- Device name
- Perifit Pump
- Applicant
- X6 Innovations FR
- Product code
- HGX — Pump, Breast, Powered
- Decision date
- 2024-01-26
- Date received
- 2023-06-20
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Obstetrics/Gynecology
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K231785.pdf
Official FDA record: K231785
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.