American Viggo - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
American Viggo has 10 FDA 510(k) cleared general hospital devices. Based in Mchenry, US.
Historical record: 10 cleared submissions from 1976 to 1977.
Browse the complete list of FDA 510(k) cleared general hospital devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - American Viggo
10 devices
Cleared
Aug 02, 1977
MALE LUER LOCK PLUG
General Hospital
14d
Cleared
Apr 29, 1977
NEEDLE, MEMBRANE
General Hospital
42d
Cleared
Mar 30, 1977
LUER-LOCK EXTENSION SET
General Hospital
63d
Cleared
Mar 30, 1977
I.V. CATHETER PLACEMENT UNIT
General Hospital
62d
Cleared
Feb 28, 1977
3-WAY STOPCOCK WITH LUER-LOCK FITTING
General & Plastic Surgery
35d
Cleared
Feb 25, 1977
EPIDURAL BLOCK PROCEDURE PACK
Anesthesiology
39d
Cleared
Dec 02, 1976
4-WAY STOPCOCK W/LUER-LOCK FITTING
General Hospital
76d
Cleared
Dec 02, 1976
4-WAY STOPCOCK W/10 CM EXTEN. TUBING
General Hospital
76d
Cleared
Dec 02, 1976
4-WAY STOPCOCK W/100 CM TUBING, LUER-LK
General Hospital
73d
Cleared
Dec 02, 1976
4-WAY STOPCOCK W/7CM TUBING,
General Hospital
73d