Cardiodynamics International Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cardiodynamics International Corp. - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Cardiodynamics International Corp. has 11 FDA 510(k) cleared cardiovascular devices. Based in San Diego, US.
Historical record: 11 cleared submissions from 1996 to 2009.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cardiodynamics International Corp.
11 devices
Cleared
May 28, 2009
CARDIODYNAMICS BIOZ RX, MODEL 7101-SYS
Cardiovascular
84d
Cleared
Sep 26, 2007
BIOZ DX HEMODYNAMIC MONITOR WITH PHILIPS 12-LEAD ECG, MODEL 5100
Cardiovascular
252d
Cleared
Jun 10, 2005
BIOZDX HEMODYNAMIC MONITOR AND 12-LEAD ECG
Cardiovascular
28d
Cleared
Dec 08, 2004
BIOZDX HEMODYNAMIC MONITOR
Cardiovascular
208d
Cleared
Nov 02, 2001
MODIFICATION TO BIOZ.COM HEMODYNAMIC MONITOR
Cardiovascular
176d
Cleared
Jul 03, 2001
BIOZTECT SENSOR AND BIOZTECT CABLE
Cardiovascular
25d
Cleared
Jun 30, 2000
BIOZ.PC HEMODYNAMIC MONITOR MODEL BZ-500/BZ-501
Cardiovascular
87d
Cleared
May 05, 2000
BIOZ.COM HEMODYNAMIC MONITOR WITH BIOZ TECT SENSOR AND BIOZ TECT CABLE...
Cardiovascular
30d
Cleared
Mar 18, 1998
BIOZ.COM SYSTEM
Cardiovascular
90d
Cleared
Sep 11, 1997
BIOZ SYSTEM & BIOZ PORTABLE
Cardiovascular
80d
Cleared
Nov 26, 1996
BIOZ SYSTEM
Cardiovascular
104d