K241833
- 510(k) number
- K241833
- Device name
- V-GRAD
- Applicant
- Vitromed GmbH DE
- Product code
- MQL — Media, Reproductive
- Decision date
- 2025-03-21
- Date received
- 2024-06-25
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Obstetrics/Gynecology
PDFDownload 510(k) SummaryArchived here · 0.3 MB · U.S. public domain
Also available from FDA: K241833.pdf
Official FDA record: K241833
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.