Clearance Summary
ARIETTA 60/ARIETTAS60/ARIETTAV60 received FDA 510(k) clearance under submission number K140443, sponsored by Hitachi Aloka Medical,Ltd. (Hitachi Aloka Medical. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2014-06-16.
- Submission: K140443
- Applicant / Sponsor: Hitachi Aloka Medical,Ltd. (Hitachi Aloka Medical
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1550
- Decision date: 2014-06-16
Classification & Regulation
This clearance is catalogued under FDA product code IYN and 21 CFR 892.1550, within the Radiology review panel as a Class II device.