Clearance Summary
Full Digital Colour Doppler Ultrasonic Diagnostic System received FDA 510(k) clearance under submission number K183041, sponsored by Wuhan Zoncare Bio-medical Electronics 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 2019-07-10.
- Submission: K183041
- Applicant / Sponsor: Wuhan Zoncare Bio-medical Electronics Co., Ltd.
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1550
- Decision date: 2019-07-10
Classification & Regulation
This clearance is catalogued under FDA product code IYN and 21 CFR 892.1550, within the Radiology review panel as a Class II device.