Clearance Summary
DELL UP3017 with QUBYX PerfectLum bundle received FDA 510(k) clearance under submission number K171229, sponsored by Qubyx Software Technologies, 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 2017-05-26.
- Submission: K171229
- Applicant / Sponsor: Qubyx Software Technologies, Inc.
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.2050
- Decision date: 2017-05-26
Classification & Regulation
This clearance is catalogued under FDA product code PGY and 21 CFR 892.2050, within the Radiology review panel as a Class II device.