Clearance Summary
LUNETTE MENSTRUAL CUP, MODELS 1 AND 2 received FDA 510(k) clearance under submission number K091754, sponsored by Lune Group , 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 2009-11-13.
- Submission: K091754
- Applicant / Sponsor: Lune Group , Ltd.
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.5400
- Decision date: 2009-11-13
Classification & Regulation
This clearance is catalogued under FDA product code HHE and 21 CFR 884.5400, within the Obstetrics/Gynecology review panel as a Class II device.