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Selectra Catheters, Selectra Accessory Kit

Page Type
Cleared 510(K)
510(k) Number
K183265
510(k) Type
Special
Applicant
Biotronik, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/13/2018
Days to Decision
20 days
Submission Type
Summary

Selectra Catheters, Selectra Accessory Kit

Page Type
Cleared 510(K)
510(k) Number
K183265
510(k) Type
Special
Applicant
Biotronik, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/13/2018
Days to Decision
20 days
Submission Type
Summary