Clearance Summary
MODIFICATION TO: HORIZON 9000WS received FDA 510(k) clearance under submission number K032997, sponsored by Mennen Medical , Ltd.. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2003-10-15.
- Submission: K032997
- Applicant / Sponsor: Mennen Medical , Ltd.
- Clearance pathway: Special
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1435
- Decision date: 2003-10-15
Classification & Regulation
This clearance is catalogued under FDA product code DXG and 21 CFR 870.1435, within the Cardiovascular review panel as a Class II device.