Clearance Summary
FORE-SIGHT CEREBRAL OXIMETER MONITOR, MODEL 2040 received FDA 510(k) clearance under submission number K061960, sponsored by Cas Medical Systems, 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 2006-09-05.
- Submission: K061960
- Applicant / Sponsor: Cas Medical Systems, Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2700
- Decision date: 2006-09-05
Classification & Regulation
This clearance is catalogued under FDA product code MUD and 21 CFR 870.2700, within the Cardiovascular review panel as a Class II device.