Clearance Summary
INTRAUTERINE INSEMINATION (IUI) CATHETER received FDA 510(k) clearance under submission number K120154, sponsored by Catheter Research, Inc.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 2012-03-21.
- Submission: K120154
- Applicant / Sponsor: Catheter Research, Inc.
- Clearance pathway: Abbreviated
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.6110
- Decision date: 2012-03-21
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.