Clearance Summary
KAEN YIH UMBILICAL CORD CLAMP received FDA 510(k) clearance under submission number K033846, sponsored by Kaen Yih Enterprise Co., Ltd.. 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 2004-03-11.
- Submission: K033846
- Applicant / Sponsor: Kaen Yih Enterprise Co., Ltd.
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.4530
- Decision date: 2004-03-11
Classification & Regulation
This clearance is catalogued under FDA product code HFW and 21 CFR 884.4530, within the Obstetrics/Gynecology review panel as a Class II device.