Cynergy is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cynergy - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Cynergy has 5 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 5 cleared submissions from 1978 to 1981. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Cynergy Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cynergy
5 devices
Cleared
Apr 01, 1981
SIEMENS MODEL 146-146A EXTERNAL PULSE G
Cardiovascular
29d
Cleared
Sep 16, 1980
CYNERGY MODEL 184
Cardiovascular
64d
Cleared
Jan 31, 1980
CYNERGY MODEL 182
Cardiovascular
55d
Cleared
Nov 30, 1979
PACESETTER MODEL 350
Cardiovascular
25d
Cleared
Sep 27, 1978
ERM-101
Cardiovascular
44d