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CARDIOMETRICS FLOWIRE 300 AND XT 300 DOPPLER GUIDE WIRES

Page Type
Cleared 510(K)
510(k) Number
K972762
510(k) Type
Traditional
Applicant
CARDIOMETRICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/14/1997
Days to Decision
82 days
Submission Type
Summary

CARDIOMETRICS FLOWIRE 300 AND XT 300 DOPPLER GUIDE WIRES

Page Type
Cleared 510(K)
510(k) Number
K972762
510(k) Type
Traditional
Applicant
CARDIOMETRICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/14/1997
Days to Decision
82 days
Submission Type
Summary