Cardio Metrics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cardio Metrics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: CARDIOMETRICS FLOWIRE 300 AND XT 300 DOPPLER GUIDE WIRES, CARDIOMETRICS WAVEWIRE/WAVEMAP PRESSURE SYSTEM, CARDIOMETICS FLOWIRE, SMARTWIRE DOPPLER GUIDE WIRE
23
Total
23
Cleared
0
Denied
Cardio Metrics, Inc. has 23 FDA 510(k) cleared cardiovascular devices. Based in Houston, US.
Historical record: 23 cleared submissions from 1986 to 1997.
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 - Cardio Metrics, Inc.
23 devices
Cleared
Oct 14, 1997
CARDIOMETRICS FLOWIRE 300 AND XT 300 DOPPLER GUIDE WIRES
Cardiovascular
82d
Cleared
Aug 18, 1997
CARDIOMETRICS WAVEWIRE/WAVEMAP PRESSURE SYSTEM
Cardiovascular
238d
Cleared
Oct 25, 1996
CARDIOMETICS FLOWIRE, SMARTWIRE DOPPLER GUIDE WIRE
Radiology
570d
Cleared
Jul 31, 1996
ACCUTRAC XT INTRAVASCULAR GUIDE WIRE (FLOPPY) MODEL 2403/(FLEX) MODEL 2404
Cardiovascular
85d
Cleared
Feb 28, 1996
CARDI0METRICS FLOW WIRE XT DOPPLER GUIDE MODEL 1403, 1404
Cardiovascular
85d
Cleared
Nov 07, 1995
CARDIOMETRICS ACCUTRAC INTRAVASCULAR GUIDE WIRE (MODIFICATION)
Cardiovascular
35d
Cleared
Aug 29, 1995
CARDIOMETRICS ACCUTRAC INTRAVASCULAR GUIDE WIRE
Cardiovascular
88d
Cleared
Sep 19, 1994
CARDIOMETRICS FLOWIRE DOPPLER GUIDE WIRE
Cardiovascular
87d
Cleared
Aug 18, 1994
CARDIOMETRICS DUALFLOW SWITCH BOX
Cardiovascular
170d
Cleared
Aug 17, 1994
CARDIOMETRICS FLOMAP AND FLOMOD ULTRASOUND INSTRUMENT
Radiology
406d
Cleared
May 31, 1994
CARDIOMETRICS FLOWIRE DOPPLER GUIDE WIRES
Cardiovascular
64d
Cleared
Sep 28, 1993
CARDIOMETRICS FLOWIRE & FLOMAP
Radiology
125d