Clearance Summary
HORIZON 9000/HIS OPTION AMPLIFIER received FDA 510(k) clearance under submission number K914381, sponsored by Mennen Medical, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1992-01-28.
- Submission: K914381
- Applicant / Sponsor: Mennen Medical, Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2050
- Decision date: 1992-01-28
Classification & Regulation
This clearance is catalogued under FDA product code DRR and 21 CFR 870.2050, within the Cardiovascular review panel as a Class II device.