Vickers America Medical Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vickers America Medical Corp. - FDA 510(k) Cleared Devices
22
Total
22
Cleared
0
Denied
Vickers America Medical Corp. has 22 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 22 cleared submissions from 1978 to 1984. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Vickers America Medical Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Vickers America Medical Corp.
22 devices
Cleared
Mar 23, 1984
TREONIC C30
General Hospital
28d
Cleared
Jan 24, 1984
LABORATORY DATA MGMT SYSTEM SDMS
Chemistry
231d
Cleared
Jun 22, 1983
RESUSCITAIRE
General Hospital
105d
Cleared
Apr 12, 1983
TREONIC IP5
General Hospital
19d
Cleared
Jan 28, 1982
OXYGENAIRE NURING INCUBATOR
General Hospital
72d
Cleared
Jan 22, 1982
NEOCARE BABY-CONTROLLED INCUBATOR
General Hospital
66d
Cleared
Jul 31, 1981
VMA PEDIATRIC APNEA MATTRESS
Anesthesiology
30d
Cleared
Apr 29, 1981
NEOCARE TEMPERATURE MONITOR
General Hospital
37d
Cleared
Mar 11, 1981
140 NEOCARE AIR CONTROLLED INCUBATOR
General Hospital
57d
Cleared
Mar 11, 1981
NEOCARE OXYGEN MONITOR
Anesthesiology
8d
Cleared
Oct 23, 1980
SP 120 SOPHISTICATE
Chemistry
37d
Cleared
Oct 03, 1980
OXFORD HUMAN MILK PASTEURISER
Obstetrics & Gynecology
128d