Clearance Summary
MORTON IUI CATHETERS received FDA 510(k) clearance under submission number K041470, sponsored by Fertility Technology Resources, Inc.. 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 2004-11-22.
- Submission: K041470
- Applicant / Sponsor: Fertility Technology Resources, Inc.
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.6110
- Decision date: 2004-11-22
Classification & Regulation
This clearance is catalogued under FDA product code MQF and 21 CFR 884.6110, within the Obstetrics/Gynecology review panel as a Class II device.