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TRANSEND 300 ES GUIDEWIRE, MODEL 46-814 & TRANSEND 300 FLOPPY GUIDEWIRE, MODEL 46-815

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022357
510(k) Type
Traditional
Applicant
Boston Scientific, Target
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/16/2002
Days to Decision
89 days
Submission Type
Summary

TRANSEND 300 ES GUIDEWIRE, MODEL 46-814 & TRANSEND 300 FLOPPY GUIDEWIRE, MODEL 46-815

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022357
510(k) Type
Traditional
Applicant
Boston Scientific, Target
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/16/2002
Days to Decision
89 days
Submission Type
Summary