Clearance Summary
MCKESSON HORIZON CARDIOLOGY received FDA 510(k) clearance under submission number K112720, sponsored by Mckesson Israel , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2012-01-30.
- Submission: K112720
- Applicant / Sponsor: Mckesson Israel , Ltd.
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.2050
- Decision date: 2012-01-30
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.