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TYPE N ENDOCARDIAL LEAD

Page Type
Cleared 510(K)
510(k) Number
K810493
510(k) Type
Traditional
Applicant
BIOTRONIK SALES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/20/1981
Days to Decision
24 days

TYPE N ENDOCARDIAL LEAD

Page Type
Cleared 510(K)
510(k) Number
K810493
510(k) Type
Traditional
Applicant
BIOTRONIK SALES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/20/1981
Days to Decision
24 days