Cardiomedics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cardiomedics, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Cardiomedics, Inc. has 5 FDA 510(k) cleared medical devices. Based in Torrance, US.
Historical record: 5 cleared submissions from 1987 to 2005. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Cardiomedics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cardiomedics, Inc.
5 devices
Cleared
Mar 31, 2005
CARDIASSIST COUNTER PULSATION SYSTEM SERIES 4000/5000
Cardiovascular
64d
Cleared
Jan 07, 2003
CARDIASSIST COUNTERPULSATION SYSTEM, MODEL MARK 3000
Cardiovascular
88d
Cleared
Aug 08, 2002
CARDIASSIST COUNTERPULSATION SYSTEM, MODEL MARK 3000
Cardiovascular
41d
Cleared
Feb 28, 2001
CARDIOMEDICS ECP SYSTEM
Cardiovascular
30d
Cleared
Sep 18, 1987
CARDIOMEDICS EXTERNAL COUNTERPULSATION SYSTEM
Cardiovascular
114d