Aloka Co. Ltd USA is one of 24549 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Aloka Co. Ltd USA - FDA 510(k) Cleared Devices
Recent clearances: ALOKA SSD-ALPHA 5 ULTRASOUND SYSTEM, ALOKA MODEL SSD-5500 V6.0 ULTRASOUND SYSTEM
2
Total
2
Cleared
0
Denied
Aloka Co. Ltd USA has 2 FDA 510(k) cleared medical devices. Based in Wallingford, US.
Historical record: 2 cleared submissions from 2003 to 2004. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Aloka Co. Ltd USA Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Aloka Co. Ltd USA
2 devices