Clearance Summary
COR ANALYZER II, MODEL V1.7 received FDA 510(k) clearance under submission number K072242, sponsored by Rcadia Medical Imaging , Ltd.. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2007-09-11.
- Submission: K072242
- Applicant / Sponsor: Rcadia Medical Imaging , Ltd.
- Clearance pathway: Special
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.2050
- Decision date: 2007-09-11
Classification & Regulation
This clearance is catalogued under FDA product code LLZ and 21 CFR 892.2050, within the Radiology review panel as a Class II device.