Clearance Summary
VERITON CT whole body SPECT/CT system received FDA 510(k) clearance under submission number K182484, sponsored by Spectrum Dynamics Medical, Ltd.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2018-11-09.
- Submission: K182484
- Applicant / Sponsor: Spectrum Dynamics Medical, Ltd.
- Clearance pathway: Abbreviated
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1200
- Decision date: 2018-11-09
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.