K232047
- 510(k) number
- K232047
- Device name
- VIVACE
- Applicant
- Unimom.Co KR
- Product code
- HGX — Pump, Breast, Powered
- Decision date
- 2024-03-28
- Date received
- 2023-07-10
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Obstetrics/Gynecology
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K232047.pdf
Official FDA record: K232047
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.