Bemiss-Jason Corp., Triad Medical Div. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bemiss-Jason Corp., Triad Medical Div. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Bemiss-Jason Corp., Triad Medical Div. has 1 FDA 510(k) cleared medical devices. Based in Waynesville, US.
Historical record: 1 cleared submissions from 1997 to 1997. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Bemiss-Jason Corp., Triad Medical Div. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Bemiss-Jason Corp., Triad Medical Div.
1 devices