Sakae Corporation is one of 14100 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sakae Corporation - FDA 510(k) Cleared Devices
Recent clearances: A1c iGear System, A1C GEAR SYSTEM
2
Total
2
Cleared
0
Denied
Sakae Corporation has 2 FDA 510(k) cleared medical devices. Based in Los Angeles, US.
Historical record: 2 cleared submissions from 2014 to 2014. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Sakae Corporation Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Ammirati Regulatory Consulting as regulatory consultant.
FDA 510(k) Regulatory Record - Sakae Corporation
2 devices