Clearance Summary
SENYINT Remote Consultation System received FDA 510(k) clearance under submission number K162727, sponsored by Dalian Senyint Digital Medical System Co., 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 2018-02-08.
- Submission: K162727
- Applicant / Sponsor: Dalian Senyint Digital Medical System Co., Ltd.
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.2050
- Decision date: 2018-02-08
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.