Clearance Summary
eUnity received FDA 510(k) clearance under submission number K161515, sponsored by Client Outlook, 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 2016-11-15.
- Submission: K161515
- Applicant / Sponsor: Client Outlook, Inc.
- Clearance pathway: Special
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.2050
- Decision date: 2016-11-15
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.