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RUBICON SUPPORT CATHETER

Page Type
Cleared 510(K)
510(k) Number
K112303
510(k) Type
Traditional
Applicant
BOSTON SCIENTIFIC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/9/2011
Days to Decision
90 days
Submission Type
Summary

RUBICON SUPPORT CATHETER

Page Type
Cleared 510(K)
510(k) Number
K112303
510(k) Type
Traditional
Applicant
BOSTON SCIENTIFIC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/9/2011
Days to Decision
90 days
Submission Type
Summary