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TYPE FH ENDOCARDIAL LEAD

Page Type
Cleared 510(K)
510(k) Number
K810494
510(k) Type
Traditional
Applicant
BIOTRONIK SALES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/7/1981
Days to Decision
164 days

TYPE FH ENDOCARDIAL LEAD

Page Type
Cleared 510(K)
510(k) Number
K810494
510(k) Type
Traditional
Applicant
BIOTRONIK SALES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/7/1981
Days to Decision
164 days