Suretone International is one of 11 FDA 510(k) medical device manufacturers from South Africa in the dataset, ranked by real submission volume.
Suretone International - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Suretone International has 1 FDA 510(k) cleared medical devices. Based in Cape Town, Cape, ZA.
Historical record: 1 cleared submissions from 2002 to 2002. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Suretone International Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Suretone International
1 devices