Last synced on 14 November 2025 at 11:06 pm

SCOUTPRO 7F CORONARY SINUS LEAD DELIVERY SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K060807
510(k) Type
Special
Applicant
Biotronik, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/24/2006
Days to Decision
31 days
Submission Type
Summary

SCOUTPRO 7F CORONARY SINUS LEAD DELIVERY SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K060807
510(k) Type
Special
Applicant
Biotronik, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/24/2006
Days to Decision
31 days
Submission Type
Summary