K232125
- 510(k) number
- K232125
- Device name
- V-PVP
- Applicant
- Vitromed GmbH DE
- Product code
- MQL — Media, Reproductive
- Decision date
- 2024-03-20
- Date received
- 2023-07-17
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Obstetrics/Gynecology
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K232125.pdf
Official FDA record: K232125
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.