Clearance Summary
DISCOVERY MR750 3.0T, DISCOVERY MR450 1.5T, DISCOVERY MR750W 3.0T, OPTIMA MR450W 1.5T received FDA 510(k) clearance under submission number K132376, sponsored by Ge Healthcare (Ge Medical Systems, LLC). The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2013-11-15.
- Submission: K132376
- Applicant / Sponsor: Ge Healthcare (Ge Medical Systems, LLC)
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1000
- Decision date: 2013-11-15
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.