K241132
- 510(k) number
- K241132
- Device name
- ARTSMedia Oocyte Aspiration Medium (502020, 502050, 502100)
- Applicant
- Artsmedia Denmark Aps DK
- Product code
- MQL — Media, Reproductive
- Decision date
- 2024-12-18
- Date received
- 2024-04-24
- 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: K241132.pdf
Official FDA record: K241132
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.