Cairco , Ltd. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Cairco , Ltd. has 9 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 9 cleared submissions from 1981 to 1982. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Cairco , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cairco , Ltd.
9 devices
Cleared
Mar 26, 1982
SHEFFIELD INFANT VENTILATOR MARK 4
Anesthesiology
156d
Cleared
Mar 12, 1982
EAST AUTOCLAVE HUMIDIFIER
Anesthesiology
142d
Cleared
Jan 22, 1982
SPIROX H
Anesthesiology
93d
Cleared
Jan 22, 1982
SPIROX A
Anesthesiology
93d
Cleared
Jan 07, 1982
EAST-FREEMAN VENTILATOR MARK 2
Anesthesiology
78d
Cleared
Dec 29, 1981
EAST WATER UNIT MARK 3
Cardiovascular
69d
Cleared
Nov 27, 1981
RADCLIFFE VENTILATOR MARK 5
Anesthesiology
37d
Cleared
Nov 16, 1981
EAST VENTILARM PRESSURE MONITOR ALARM S.
Anesthesiology
26d
Cleared
Apr 17, 1981
POLARISED LIGHT GRONIOMETER
Neurology
38d