Clearance Summary
OMNI-VUE 2 SYSTEM received FDA 510(k) clearance under submission number K130374, sponsored by Genesis Digital Imaging, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2013-08-29.
- Submission: K130374
- Applicant / Sponsor: Genesis Digital Imaging, Inc.
- Clearance pathway: Special
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.2050
- Decision date: 2013-08-29
Classification & Regulation
This clearance is catalogued under FDA product code LLZ and 21 CFR 892.2050, within the Radiology review panel as a Class II device.