Clearance Summary
CSI MODEL 5K MANAGED HEALTH SYSTEM KIOSK received FDA 510(k) clearance under submission number K093389, sponsored by Computerized Screening, 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 2009-11-17.
- Submission: K093389
- Applicant / Sponsor: Computerized Screening, Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1130
- Decision date: 2009-11-17
Classification & Regulation
This clearance is catalogued under FDA product code DXN and 21 CFR 870.1130, within the Cardiovascular review panel as a Class II device.