FDA 510(k) Applications Submitted by CARDIOMETRICS, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K961777 05/07/1996 ACCUTRAC XT INTRAVASCULAR GUIDE WIRE (FLOPPY) MODEL 2403/(FLEX) MODEL 2404 CARDIOMETRICS, INC.
K972762 07/24/1997 CARDIOMETRICS FLOWIRE 300 AND XT 300 DOPPLER GUIDE WIRES CARDIOMETRICS, INC.
K965140 12/23/1996 CARDIOMETRICS WAVEWIRE/WAVEMAP PRESSURE SYSTEM CARDIOMETRICS, INC.
K955551 12/05/1995 CARDI0METRICS FLOW WIRE XT DOPPLER GUIDE MODEL 1403, 1404 CARDIOMETRICS, INC.
K951567 04/04/1995 CARDIOMETICS FLOWIRE, SMARTWIRE DOPPLER GUIDE WIRE CARDIOMETRICS, INC.


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