Cardiocomm Solutions, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Cardiocomm Solutions, Inc. - FDA 510(k) Cleared Devices
Recent clearances: HeartCheck Cardi Beat ECG Monitor with GEMS Mobile
9
Total
9
Cleared
0
Denied
Cardiocomm Solutions, Inc. has 9 FDA 510(k) cleared medical devices. Based in Victoria, B.C., CA.
Historical record: 9 cleared submissions from 2002 to 2019. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Cardiocomm Solutions, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cardiocomm Solutions, Inc.
9 devices
Cleared
Feb 22, 2019
HeartCheck Cardi Beat ECG Monitor with GEMS Mobile
Cardiovascular
281d
Cleared
Feb 11, 2014
GUAVA II
Cardiovascular
531d
Cleared
May 17, 2012
HEARTCHECK ECG PEN WITH GEMS HOME
Cardiovascular
44d
Cleared
Dec 22, 2011
HEARTCHECK PEN HANDHELD ECG WITH GEMS HOME
Cardiovascular
241d
Cleared
Oct 07, 2011
GLOBALCARDIO
Cardiovascular
150d
Cleared
Oct 31, 2003
MODIFICATION TO GLOBALCARDIO
Cardiovascular
32d
Cleared
Sep 27, 2002
GLOBAL ECG MANAGEMENT SYSTEM (GEMS)
Cardiovascular
73d
Cleared
Apr 30, 2002
GLOBAL ECG MANAGEMENT SYSTEM (GEMS)
Cardiovascular
85d
Cleared
Jan 31, 2002
GLOBALCARDIO
Cardiovascular
114d