Clearance Summary
ALOKA SSD-2000 DIAGNOSTIC ULTRASOUND SYSTEM MODIFICATION received FDA 510(k) clearance under submission number K941652, sponsored by Aloka 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 1994-10-21.
- Submission: K941652
- Applicant / Sponsor: Aloka Co., Ltd.
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1550
- Decision date: 1994-10-21
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.