Clearance Summary
HUDSON 2020, 2040, 2060,ULTRASOUND SCANNERS received FDA 510(k) clearance under submission number K022928, sponsored by Hudson Diagnostic Imaging, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2002-12-11.
- Submission: K022928
- Applicant / Sponsor: Hudson Diagnostic Imaging, LLC
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1560
- Decision date: 2002-12-11
Classification & Regulation
This clearance is catalogued under FDA product code IYO and 21 CFR 892.1560, within the Radiology review panel as a Class II device.