Clearance Summary
AIRIS MAGNETIC RESONANCE DIAGNOSTIC DEVICE received FDA 510(k) clearance under submission number K980691, sponsored by Hitachi Medical Systems America, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1998-05-11.
- Submission: K980691
- Applicant / Sponsor: Hitachi Medical Systems America, Inc.
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1000
- Decision date: 1998-05-11
Classification & Regulation
This clearance is catalogued under FDA product code MOS and 21 CFR 892.1000, within the Radiology review panel as a Class II device.