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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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