Clearance Summary
MAGNETIC RESONANCE DEVICE ACCESSORY received FDA 510(k) clearance under submission number K911276, sponsored by Toshiba America Mri, 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 1991-06-28.
- Submission: K911276
- Applicant / Sponsor: Toshiba America Mri, Inc.
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1000
- Decision date: 1991-06-28
Classification & Regulation
This clearance is catalogued under FDA product code LNH and 21 CFR 892.1000, within the Radiology review panel as a Class II device.