Venospital, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Venospital, Inc. - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
Venospital, Inc. has 14 FDA 510(k) cleared general hospital devices. Based in Mchenry, US.
Historical record: 14 cleared submissions from 1977 to 1979.
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 - Venospital, Inc.
14 devices
Cleared
Sep 04, 1979
FLU-VEN TK-2
Hematology
78d
Cleared
Sep 04, 1979
FLU VEN TR-1
Hematology
78d
Cleared
Apr 30, 1979
BIOSTIL # 3884
General Hospital
109d
Cleared
Apr 30, 1979
FLU-VEN 01510
General Hospital
60d
Cleared
Aug 10, 1978
INFUSION SET, VENOTHIN 19
General Hospital
27d
Cleared
Aug 10, 1978
INFUSION SET W/ INJECTION SITE
General Hospital
27d
Cleared
Aug 10, 1978
INFUSION, VENOTHIN 23
General Hospital
27d
Cleared
Aug 10, 1978
INFUSION SET W/ INJECTION SITE, 23D-W
General Hospital
27d
Cleared
Aug 10, 1978
INFUSION SET, VENOTHIN 25
General Hospital
27d
Cleared
Aug 10, 1978
FLU VEN 0151
General Hospital
27d
Cleared
Aug 10, 1978
INFUSION SET, VENOTHIN 21
General Hospital
27d
Cleared
Aug 22, 1977
FLU VEN 0150
General Hospital
35d
Cleared
Jun 24, 1977
HEMODIALYSIS FISTULA SET
Gastroenterology & Urology
44d
Cleared
Jun 14, 1977
FLU VEN 0160
General Hospital
34d