Curacloud Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Curacloud Corp. - FDA 510(k) Cleared Devices
Recent clearances: CuraRad-ICH
1
Total
1
Cleared
0
Denied
Curacloud Corp. has 1 FDA 510(k) cleared medical devices. Based in Seattle, US.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Curacloud Corp. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Manatt, Phelps, & Phillips, Llp as regulatory consultant.
FDA 510(k) Regulatory Record - Curacloud Corp.
1 devices