Clearance Summary
CHEETAH RELIANT, CHEETAH ACTIVE received FDA 510(k) clearance under submission number K072662, sponsored by Cheetah 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 2008-01-16.
- Submission: K072662
- Applicant / Sponsor: Cheetah Medical, Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2770
- Decision date: 2008-01-16
Classification & Regulation
This clearance is catalogued under FDA product code DSB and 21 CFR 870.2770, within the Cardiovascular review panel as a Class II device.