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FATHOM 16 STEERABLE GUIDEWIRE MODEL M001509XXX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K111485
510(k) Type
Traditional
Applicant
Boston Scientific Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/30/2011
Days to Decision
30 days
Submission Type
Summary

FATHOM 16 STEERABLE GUIDEWIRE MODEL M001509XXX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K111485
510(k) Type
Traditional
Applicant
Boston Scientific Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/30/2011
Days to Decision
30 days
Submission Type
Summary