Last synced on 18 April 2025 at 11:05 pm

CARDIOMETRICS FLOWIRE 300 AND XT 300 DOPPLER GUIDE WIRES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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