Debusk Technology Corp. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Debusk Technology Corp. has 4 FDA 510(k) cleared medical devices. Based in Knoxville, US.
Historical record: 4 cleared submissions from 1994 to 1996. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Debusk Technology Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Debusk Technology Corp.
4 devices
Cleared
Jul 03, 1996
DEROYAL INDUSTRIES, INC. NEONATAL EYE COVER
General Hospital
19d
Cleared
May 06, 1994
TROCAR AND CANNULA
General & Plastic Surgery
52d
Cleared
May 02, 1994
ELECTROSURGICAL DISPERSIVE ELECTRODE AND ELECTROSURGICAL DUAL RETURN...
General & Plastic Surgery
101d
Cleared
Mar 30, 1994
ELECTROSURGICAL MONOPOLAR HANDSWITCHING PENCIL W/REMOVABLE BLADE
General & Plastic Surgery
35d