Viggo Products is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Viggo Products - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Viggo Products has 7 FDA 510(k) cleared medical devices. Based in Madison, US.
Historical record: 7 cleared submissions from 1985 to 1985. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Viggo Products Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Viggo Products
7 devices
Cleared
May 29, 1985
VIGGO ACCESSORIES FOR I.V. THERAPY
General Hospital
93d
Cleared
Apr 12, 1985
VIGGO NEOFLON INFUSION CANNULA
General Hospital
79d
Cleared
Apr 12, 1985
VIGGO I.V. ACCESSORIES-VIGGO EXTENSION TUBES ETC.
General Hospital
79d
Cleared
Apr 11, 1985
VIGGO CONNECTA 3-WAY INFUSION STOPCOCK
General Hospital
78d
Cleared
Apr 11, 1985
VIGGO SECALON T CATHETER
General Hospital
64d
Cleared
Apr 09, 1985
VASCULON I.V. CANNULAE
General Hospital
76d
Cleared
Apr 09, 1985
VIGGO ARTERIAL CANNULA
General Hospital
71d