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LEPTOS PULSE GENERATOR

Page Type
Cleared 510(K)
510(k) Number
K844794
510(k) Type
Traditional
Applicant
BIOTRONIK SALES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/18/1985
Days to Decision
129 days

LEPTOS PULSE GENERATOR

Page Type
Cleared 510(K)
510(k) Number
K844794
510(k) Type
Traditional
Applicant
BIOTRONIK SALES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/18/1985
Days to Decision
129 days