Cloudcath is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cloudcath - FDA 510(k) Cleared Devices
Recent clearances: CloudCath Peritoneal Dialysis Drain Set Monitoring System
1
Total
1
Cleared
0
Denied
Cloudcath has 1 FDA 510(k) cleared medical devices. Based in San Francisco, US.
Last cleared in 2022. Active since 2022. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Cloudcath Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Cloudcath
1 devices