Last synced on 14 November 2025 at 11:06 pm

Selectra 3D Outer Guiding Catheters

Page Type
Cleared 510(K)
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)
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