Clearance Summary
GENUA MENOPAUSE MONITOR TEST KIT received FDA 510(k) clearance under submission number K002450, sponsored by Genua 1944, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 2001-01-12.
- Submission: K002450
- Applicant / Sponsor: Genua 1944, Inc.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class I
- Regulation citation: 21 CFR 862.1300
- Decision date: 2001-01-12
Classification & Regulation
This clearance is catalogued under FDA product code CGJ and 21 CFR 862.1300, within the Clinical Chemistry review panel as a Class I device.