Jolife AB - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
FDA 510(k) Regulatory Record - Jolife AB Cardiovascular ✕
5 devices
Cleared
Feb 08, 2018
LUCAS 3 Chest Compression System
Cardiovascular
84d
Cleared
Nov 09, 2016
LUCAS 3 Chest Compression System
Cardiovascular
135d
Cleared
Jun 17, 2009
LUCAS 2
Cardiovascular
119d
Cleared
Sep 28, 2006
MODIFICATION TO LUCAS
Cardiovascular
43d
Cleared
Feb 01, 2006
LUCAS
Cardiovascular
57d