Cygnus Research Corp. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Cygnus Research Corp. has 5 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 5 cleared submissions from 1983 to 1983. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Cygnus Research Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cygnus Research Corp.
5 devices
Cleared
Jul 19, 1983
VAPOR-PHASE HUMIDIFIER SYSTEM
Anesthesiology
64d
Cleared
May 03, 1983
TEMP-CHECK ADAPTOR, STRAIGHT CONFIGURA
Anesthesiology
42d
Cleared
May 03, 1983
LO-COMP RESERVOIR-RE-1000
Anesthesiology
22d
Cleared
May 02, 1983
TEMP-CHECK ADAPTOR, Y-CONFIGURATION
Anesthesiology
41d
Cleared
May 02, 1983
TEMP-CHECK ADAPTOR, TEE-CONFIGURATION
Anesthesiology
41d