Clearance Summary
PROBEAT WITH MGCS received FDA 510(k) clearance under submission number K060834, sponsored by Hitachi , 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 2006-04-19.
- Submission: K060834
- Applicant / Sponsor: Hitachi , Ltd.
- Clearance pathway: Special
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.5050
- Decision date: 2006-04-19
Classification & Regulation
This clearance is catalogued under FDA product code LHN and 21 CFR 892.5050, within the Radiology review panel as a Class II device.