K242640
- 510(k) number
- K242640
- Device name
- FertiCult Flushing medium; FertiCult Flushing medium with phenol red and gentamicin
- Applicant
- Fertipro NV BE
- Product code
- MQL — Media, Reproductive
- Decision date
- 2025-05-30
- Date received
- 2024-09-03
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Obstetrics/Gynecology
PDFDownload 510(k) SummaryArchived here · 0.7 MB · U.S. public domain
Also available from FDA: K242640.pdf
Official FDA record: K242640
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.