Clearance Summary
VITRIFICATION KIT & VITRIFICATION WARMING KIT received FDA 510(k) clearance under submission number K073522, sponsored by Sage In-Vitro Fertilization, 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 2008-10-10.
- Submission: K073522
- Applicant / Sponsor: Sage In-Vitro Fertilization, Inc.
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.6180
- Decision date: 2008-10-10
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.