Clearance Summary
UC-CARE NaviGo Workstation received FDA 510(k) clearance under submission number K160934, sponsored by UC-CARE , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2017-02-06.
- Submission: K160934
- Applicant / Sponsor: UC-CARE , Ltd.
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.2050
- Decision date: 2017-02-06
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.