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Selectra 3D Outer Guiding Catheters

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K193474
510(k) Type
Traditional
Applicant
Biotronik, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/16/2020
Days to Decision
305 days
Submission Type
Summary

Selectra 3D Outer Guiding Catheters

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K193474
510(k) Type
Traditional
Applicant
Biotronik, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/16/2020
Days to Decision
305 days
Submission Type
Summary