Fukuda Denshi Co., Ltd. is one of 24586 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Fukuda Denshi Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: UF-760AG, UF-870 AG DIAGNOSTIC ULTRASOUND SYSTEM
2
Total
2
Cleared
0
Denied
Fukuda Denshi Co., Ltd. has 2 FDA 510(k) cleared medical devices. Based in Redmond, US.
Historical record: 2 cleared submissions from 2008 to 2011. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Fukuda Denshi Co., Ltd. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Citech and Regulatory Technology Services, LLC.
FDA 510(k) Regulatory Record - Fukuda Denshi Co., Ltd.
2 devices