Stethocloud Pty.Ltd (Clinicloud) is one of 80 FDA 510(k) medical device manufacturers from Australia in the dataset, ranked by real submission volume.
Stethocloud Pty.Ltd (Clinicloud) - FDA 510(k) Cleared Devices
Recent clearances: CliniCloud Stethoscope
2
Total
2
Cleared
0
Denied
Stethocloud Pty.Ltd (Clinicloud) has 2 FDA 510(k) cleared medical devices. Based in Melbourne Vic, AU.
Historical record: 2 cleared submissions from 2016 to 2018. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Stethocloud Pty.Ltd (Clinicloud) Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Third Party Review Group, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Stethocloud Pty.Ltd (Clinicloud)
2 devices