Victus, Inc. is one of 21683 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Victus, Inc. - FDA 510(k) Cleared Devices
Recent clearances: EXTENSION SET (STANDARDBORE TUBING), EXTENSION SET (MINIBORE TUBING), IV ADMINISTRATION SET ( STANDARD, VICTUS I.V. ADMINISTRATION SET, MODELS 27071 AND 27072, VICTUS I.V. ADMINISTRATION SET, MODELS 27058, 27059,27062
3
Total
3
Cleared
0
Denied
Victus, Inc. has 3 FDA 510(k) cleared medical devices. Based in Miami, US.
Historical record: 3 cleared submissions from 2002 to 2010. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Victus, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Victus, Inc.
3 devices
Cleared
Jan 27, 2010
EXTENSION SET (STANDARDBORE TUBING), EXTENSION SET (MINIBORE TUBING), IV...
General Hospital
100d
Cleared
Feb 26, 2003
VICTUS I.V. ADMINISTRATION SET, MODELS 27071 AND 27072
General Hospital
33d
Cleared
Dec 10, 2002
VICTUS I.V. ADMINISTRATION SET, MODELS 27058, 27059,27062
General Hospital
55d