Clearance Summary
QUALIS received FDA 510(k) clearance under submission number K133295, sponsored by Menicon Co., Ltd. New Business Division. 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 2014-06-18.
- Submission: K133295
- Applicant / Sponsor: Menicon Co., Ltd. New Business Division
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.6160
- Decision date: 2014-06-18
Classification & Regulation
This clearance is catalogued under FDA product code MQK and 21 CFR 884.6160, within the Obstetrics/Gynecology review panel as a Class II device.