Clearance Summary
MODIFICATION TO WBR, MODEL HR received FDA 510(k) clearance under submission number K031874, sponsored by U.C.G. Technologies , Ltd.. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2003-07-18.
- Submission: K031874
- Applicant / Sponsor: U.C.G. Technologies , Ltd.
- Clearance pathway: Special
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1200
- Decision date: 2003-07-18
Classification & Regulation
This clearance is catalogued under FDA product code KPS and 21 CFR 892.1200, within the Radiology review panel as a Class II device.