Clearance Summary
SSD-1000 DIAGNOSTIC ULTRASOUND SYSTEM received FDA 510(k) clearance under submission number K012253, sponsored by Aloka Co., 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 2001-08-30.
- Submission: K012253
- Applicant / Sponsor: Aloka Co., Ltd.
- Clearance pathway: Abbreviated
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1560
- Decision date: 2001-08-30
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.