Clearance Summary
CEROX MODEL 3210 received FDA 510(k) clearance under submission number K093923, sponsored by Or-Nim 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 2010-01-19.
- Submission: K093923
- Applicant / Sponsor: Or-Nim Medical , Ltd.
- Clearance pathway: Special
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2700
- Decision date: 2010-01-19
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.