Clearance Summary
ARTSMedia Semen Wash Medium received FDA 510(k) clearance under submission number K241095, sponsored by Artsmedia Denmark Aps. The device was reviewed via the Traditional premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 2024-12-18.
- Submission: K241095
- Applicant / Sponsor: Artsmedia Denmark Aps
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.6180
- Decision date: 2024-12-18
Classification & Regulation
This clearance is catalogued under FDA product code MQL and 21 CFR 884.6180, within the Obstetrics/Gynecology review panel as a Class II device.