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ACCUTRAC XT INTRAVASCULAR GUIDE WIRE (FLOPPY) MODEL 2403/(FLEX) MODEL 2404

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K961777
510(k) Type
Traditional
Applicant
CARDIOMETRICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/31/1996
Days to Decision
85 days
Submission Type
Summary

ACCUTRAC XT INTRAVASCULAR GUIDE WIRE (FLOPPY) MODEL 2403/(FLEX) MODEL 2404

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K961777
510(k) Type
Traditional
Applicant
CARDIOMETRICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/31/1996
Days to Decision
85 days
Submission Type
Summary